{
    "items": [
        "\n\n    <div class=\"listing-item listing-item-publication\" itemscope itemprop=\"itemListElement\" itemtype=\"http://schema.org/PublicationVolume\">\n\n        <div class=\"row\">\n\n            \n\n            <div class=\"col-xs-12\">\n                            \n                \n                    <div class=\"pull-right\">\n                        <div class=\"altmetric-embed\" data-badge-popover=\"top\" data-badge-type=\"donut\" data-doi=\"10.1016/j.ajhg.2013.11.020\" data-hide-no-mentions=\"true\" data-link-target=\"_blank\"></div>\n                    </div>\n                \n            \n                <h2 class=\"media-heading\">\n                    <a href=\"https://www.rdm.ox.ac.uk/publications/444123\" title=\"A noncoding expansion in EIF4A3 causes Richieri-Costa-Pereira syndrome, a craniofacial disorder associated with limb defects.\" data-toggle=\"modal\" data-target=\"#modal\" itemprop=\"name\" data-href=\"https://www.rdm.ox.ac.uk/publications/444123/@@modal\" class=\"state-synced\">A noncoding expansion in EIF4A3 causes Richieri-Costa-Pereira syndrome, a craniofacial disorder associated with limb defects.</a>\n                </h2>\n  \n                \n                    <p class=\"categories-list\">\n                        \n                            <span class=\"label label-primary\">Journal article</span>\n                        \n                    </p>\n                \n\n                \n                \n                        \n                    <p itemprop=\"description\">Favaro FP. et al, (2014), Am J Hum Genet, 94, 120 - 128</p>\n                \n                        \n                \n                    <p>\n                        \n                    </p>\n                \n                \n            </div>\n\n        </div>\n\n    </div>\n\n\n", 
        "\n\n    <div class=\"listing-item listing-item-publication\" itemscope itemprop=\"itemListElement\" itemtype=\"http://schema.org/PublicationVolume\">\n\n        <div class=\"row\">\n\n            \n\n            <div class=\"col-xs-12\">\n                            \n                \n                    <div class=\"pull-right\">\n                        <div class=\"altmetric-embed\" data-badge-popover=\"top\" data-badge-type=\"donut\" data-doi=\"10.1186/s12881-014-0095-4\" data-hide-no-mentions=\"true\" data-link-target=\"_blank\"></div>\n                    </div>\n                \n            \n                <h2 class=\"media-heading\">\n                    <a href=\"https://www.rdm.ox.ac.uk/publications/489383\" title=\"Apparently synonymous substitutions in FGFR2 affect splicing and result in mild Crouzon syndrome.\" data-toggle=\"modal\" data-target=\"#modal\" itemprop=\"name\" data-href=\"https://www.rdm.ox.ac.uk/publications/489383/@@modal\" class=\"state-synced\">Apparently synonymous substitutions in FGFR2 affect splicing and result in mild Crouzon syndrome.</a>\n                </h2>\n  \n                \n                    <p class=\"categories-list\">\n                        \n                            <span class=\"label label-primary\">Journal article</span>\n                        \n                    </p>\n                \n\n                \n                \n                        \n                    <p itemprop=\"description\">Fenwick AL. et al, (2014), BMC medical genetics, 15</p>\n                \n                        \n                \n                    <p>\n                        \n                    </p>\n                \n                \n            </div>\n\n        </div>\n\n    </div>\n\n\n", 
        "\n\n    <div class=\"listing-item listing-item-publication\" itemscope itemprop=\"itemListElement\" itemtype=\"http://schema.org/PublicationVolume\">\n\n        <div class=\"row\">\n\n            \n\n            <div class=\"col-xs-12\">\n                            \n                \n                    <div class=\"pull-right\">\n                        <div class=\"altmetric-embed\" data-badge-popover=\"top\" data-badge-type=\"donut\" data-doi=\"10.1136/jmedgenet-2014-102573\" data-hide-no-mentions=\"true\" data-link-target=\"_blank\"></div>\n                    </div>\n                \n            \n                <h2 class=\"media-heading\">\n                    <a href=\"https://www.rdm.ox.ac.uk/publications/492377\" title=\"Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism\" data-toggle=\"modal\" data-target=\"#modal\" itemprop=\"name\" data-href=\"https://www.rdm.ox.ac.uk/publications/492377/@@modal\" class=\"state-synced\">Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism</a>\n                </h2>\n  \n                \n                    <p class=\"categories-list\">\n                        \n                            <span class=\"label label-primary\">Journal article</span>\n                        \n                    </p>\n                \n\n                \n                \n                        \n                    <p itemprop=\"description\">Ansari M. et al, (2014), Journal of Medical Genetics, 51, 659 - 668</p>\n                \n                        \n                \n                    <p>\n                        \n                    </p>\n                \n                \n            </div>\n\n        </div>\n\n    </div>\n\n\n", 
        "\n\n    <div class=\"listing-item listing-item-publication\" itemscope itemprop=\"itemListElement\" itemtype=\"http://schema.org/PublicationVolume\">\n\n        <div class=\"row\">\n\n            \n\n            <div class=\"col-xs-12\">\n                            \n                \n                    <div class=\"pull-right\">\n                        <div class=\"altmetric-embed\" data-badge-popover=\"top\" data-badge-type=\"donut\" data-doi=\"10.1038/ejhg.2013.273\" data-hide-no-mentions=\"true\" data-link-target=\"_blank\"></div>\n                    </div>\n                \n            \n                <h2 class=\"media-heading\">\n                    <a href=\"https://www.rdm.ox.ac.uk/publications/478396\" title=\"Phenotypes of craniofrontonasal syndrome in patients with a pathogenic mutation in EFNB1\" data-toggle=\"modal\" data-target=\"#modal\" itemprop=\"name\" data-href=\"https://www.rdm.ox.ac.uk/publications/478396/@@modal\" class=\"state-synced\">Phenotypes of craniofrontonasal syndrome in patients with a pathogenic mutation in EFNB1</a>\n                </h2>\n  \n                \n                    <p class=\"categories-list\">\n                        \n                            <span class=\"label label-primary\">Journal article</span>\n                        \n                    </p>\n                \n\n                \n                \n                        \n                    <p itemprop=\"description\">Van Den Elzen MEP. et al, (2014), European Journal of Human Genetics, 22, 995 - 1001</p>\n                \n                        \n                \n                    <p>\n                        \n                    </p>\n                \n                \n            </div>\n\n        </div>\n\n    </div>\n\n\n", 
        "\n\n    <div class=\"listing-item listing-item-publication\" itemscope itemprop=\"itemListElement\" itemtype=\"http://schema.org/PublicationVolume\">\n\n        <div class=\"row\">\n\n            \n\n            <div class=\"col-xs-12\">\n                            \n                \n                    <div class=\"pull-right\">\n                        <div class=\"altmetric-embed\" data-badge-popover=\"top\" data-badge-type=\"donut\" data-doi=\"10.1093/nar/gkt1026\" data-hide-no-mentions=\"true\" data-link-target=\"_blank\"></div>\n                    </div>\n                \n            \n                <h2 class=\"media-heading\">\n                    <a href=\"https://www.rdm.ox.ac.uk/publications/438723\" title=\"The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data.\" data-toggle=\"modal\" data-target=\"#modal\" itemprop=\"name\" data-href=\"https://www.rdm.ox.ac.uk/publications/438723/@@modal\" class=\"state-synced\">The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data.</a>\n                </h2>\n  \n                \n                    <p class=\"categories-list\">\n                        \n                            <span class=\"label label-primary\">Journal article</span>\n                        \n                    </p>\n                \n\n                \n                \n                        \n                    <p itemprop=\"description\">K\u00f6hler S. et al, (2014), Nucleic Acids Res, 42, D966 - D974</p>\n                \n                        \n                \n                    <p>\n                        \n                    </p>\n                \n                \n            </div>\n\n        </div>\n\n    </div>\n\n\n", 
        "\n\n    <div class=\"listing-item listing-item-publication\" itemscope itemprop=\"itemListElement\" itemtype=\"http://schema.org/PublicationVolume\">\n\n        <div class=\"row\">\n\n            \n\n            <div class=\"col-xs-12\">\n                            \n                \n                    <div class=\"pull-right\">\n                        <div class=\"altmetric-embed\" data-badge-popover=\"top\" data-badge-type=\"donut\" data-doi=\"10.1073/pnas.1311381110\" data-hide-no-mentions=\"true\" data-link-target=\"_blank\"></div>\n                    </div>\n                \n            \n                <h2 class=\"media-heading\">\n                    <a href=\"https://www.rdm.ox.ac.uk/publications/440163\" title=\"Contributions of intrinsic mutation rate and selfish selection to levels of de novo HRAS mutations in the paternal germline.\" data-toggle=\"modal\" data-target=\"#modal\" itemprop=\"name\" data-href=\"https://www.rdm.ox.ac.uk/publications/440163/@@modal\" class=\"state-synced\">Contributions of intrinsic mutation rate and selfish selection to levels of de novo HRAS mutations in the paternal germline.</a>\n                </h2>\n  \n                \n                    <p class=\"categories-list\">\n                        \n                            <span class=\"label label-primary\">Journal article</span>\n                        \n                    </p>\n                \n\n                \n                \n                        \n                    <p itemprop=\"description\">Giannoulatou E. et al, (2013), Proc Natl Acad Sci U S A, 110, 20152 - 20157</p>\n                \n                        \n                \n                    <p>\n                        \n                    </p>\n                \n                \n            </div>\n\n        </div>\n\n    </div>\n\n\n", 
        "\n\n    <div class=\"listing-item listing-item-publication\" itemscope itemprop=\"itemListElement\" itemtype=\"http://schema.org/PublicationVolume\">\n\n        <div class=\"row\">\n\n            \n\n            <div class=\"col-xs-12\">\n                            \n                \n                    <div class=\"pull-right\">\n                        <div class=\"altmetric-embed\" data-badge-popover=\"top\" data-badge-type=\"donut\" data-doi=\"10.1177/0022034513507954\" data-hide-no-mentions=\"true\" data-link-target=\"_blank\"></div>\n                    </div>\n                \n            \n                <h2 class=\"media-heading\">\n                    <a href=\"https://www.rdm.ox.ac.uk/publications/827531\" title=\"Translational genetics: advancing fronts for craniofacial health.\" data-toggle=\"modal\" data-target=\"#modal\" itemprop=\"name\" data-href=\"https://www.rdm.ox.ac.uk/publications/827531/@@modal\" class=\"state-synced\">Translational genetics: advancing fronts for craniofacial health.</a>\n                </h2>\n  \n                \n                    <p class=\"categories-list\">\n                        \n                            <span class=\"label label-primary\">Journal article</span>\n                        \n                    </p>\n                \n\n                \n                \n                        \n                    <p itemprop=\"description\">D'Souza RN. et al, (2013), J Dent Res, 92, 1058 - 1064</p>\n                \n                        \n                \n                    <p>\n                        \n                    </p>\n                \n                \n            </div>\n\n        </div>\n\n    </div>\n\n\n", 
        "\n\n    <div class=\"listing-item listing-item-publication\" itemscope itemprop=\"itemListElement\" itemtype=\"http://schema.org/PublicationVolume\">\n\n        <div class=\"row\">\n\n            \n\n            <div class=\"col-xs-12\">\n                            \n                \n                    <div class=\"pull-right\">\n                        <div class=\"altmetric-embed\" data-badge-popover=\"top\" data-badge-type=\"donut\" data-doi=\"10.1038/ng1013-1261a\" data-hide-no-mentions=\"true\" data-link-target=\"_blank\"></div>\n                    </div>\n                \n            \n                <h2 class=\"media-heading\">\n                    <a href=\"https://www.rdm.ox.ac.uk/publications/431232\" title=\"Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis.\" data-toggle=\"modal\" data-target=\"#modal\" itemprop=\"name\" data-href=\"https://www.rdm.ox.ac.uk/publications/431232/@@modal\" class=\"state-synced\">Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis.</a>\n                </h2>\n  \n                \n                    <p class=\"categories-list\">\n                        \n                            <span class=\"label label-primary\">Journal article</span>\n                        \n                    </p>\n                \n\n                \n                \n                        \n                    <p itemprop=\"description\">Sharma VP. et al, (2013), Nat Genet, 45</p>\n                \n                        \n                \n                    <p>\n                        \n                    </p>\n                \n                \n            </div>\n\n        </div>\n\n    </div>\n\n\n", 
        "\n\n    <div class=\"listing-item listing-item-publication\" itemscope itemprop=\"itemListElement\" itemtype=\"http://schema.org/PublicationVolume\">\n\n        <div class=\"row\">\n\n            \n\n            <div class=\"col-xs-12\">\n                            \n                \n                    <div class=\"pull-right\">\n                        <div class=\"altmetric-embed\" data-badge-popover=\"top\" data-badge-type=\"donut\" data-doi=\"10.3324/haematol.2013.089490\" data-hide-no-mentions=\"true\" data-link-target=\"_blank\"></div>\n                    </div>\n                \n            \n                <h2 class=\"media-heading\">\n                    <a href=\"https://www.rdm.ox.ac.uk/publications/401168\" title=\"Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type I.\" data-toggle=\"modal\" data-target=\"#modal\" itemprop=\"name\" data-href=\"https://www.rdm.ox.ac.uk/publications/401168/@@modal\" class=\"state-synced\">Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type I.</a>\n                </h2>\n  \n                \n                    <p class=\"categories-list\">\n                        \n                            <span class=\"label label-primary\">Journal article</span>\n                        \n                    </p>\n                \n\n                \n                \n                        \n                    <p itemprop=\"description\">Babbs C. et al, (2013), Haematologica, 98, 1383 - 1387</p>\n                \n                        \n                \n                    <p>\n                        \n                    </p>\n                \n                \n            </div>\n\n        </div>\n\n    </div>\n\n\n", 
        "\n\n    <div class=\"listing-item listing-item-publication\" itemscope itemprop=\"itemListElement\" itemtype=\"http://schema.org/PublicationVolume\">\n\n        <div class=\"row\">\n\n            \n\n            <div class=\"col-xs-12\">\n                            \n                \n                    <div class=\"pull-right\">\n                        <div class=\"altmetric-embed\" data-badge-popover=\"top\" data-badge-type=\"donut\" data-doi=\"10.1038/ejhg.2013.91\" data-hide-no-mentions=\"true\" data-link-target=\"_blank\"></div>\n                    </div>\n                \n            \n                <h2 class=\"media-heading\">\n                    <a href=\"https://www.rdm.ox.ac.uk/publications/388173\" title=\"Next-generation sequencing (NGS) as a diagnostic tool for retinal degeneration reveals a much higher detection rate in early-onset disease.\" data-toggle=\"modal\" data-target=\"#modal\" itemprop=\"name\" data-href=\"https://www.rdm.ox.ac.uk/publications/388173/@@modal\" class=\"state-synced\">Next-generation sequencing (NGS) as a diagnostic tool for retinal degeneration reveals a much higher detection rate in early-onset disease.</a>\n                </h2>\n  \n                \n                    <p class=\"categories-list\">\n                        \n                            <span class=\"label label-primary\">Journal article</span>\n                        \n                    </p>\n                \n\n                \n                \n                        \n                    <p itemprop=\"description\">Shanks ME. et al, (2013), Eur J Hum Genet, 21</p>\n                \n                        \n                \n                    <p>\n                        \n                    </p>\n                \n                \n            </div>\n\n        </div>\n\n    </div>\n\n\n", 
        "\n\n    <div class=\"listing-item listing-item-publication\" itemscope itemprop=\"itemListElement\" itemtype=\"http://schema.org/PublicationVolume\">\n\n        <div class=\"row\">\n\n            \n\n            <div class=\"col-xs-12\">\n                            \n                \n                    <div class=\"pull-right\">\n                        <div class=\"altmetric-embed\" data-badge-popover=\"top\" data-badge-type=\"donut\" data-doi=\"10.1176/appi.ajp.2013.12101352\" data-hide-no-mentions=\"true\" data-link-target=\"_blank\"></div>\n                    </div>\n                \n            \n                <h2 class=\"media-heading\">\n                    <a href=\"https://www.rdm.ox.ac.uk/publications/401982\" title=\"&quot;Selfish spermatogonial selection&quot;: a novel mechanism for the association between advanced paternal age and neurodevelopmental disorders.\" data-toggle=\"modal\" data-target=\"#modal\" itemprop=\"name\" data-href=\"https://www.rdm.ox.ac.uk/publications/401982/@@modal\" class=\"state-synced\">\"Selfish spermatogonial selection\": a novel mechanism for the association between advanced paternal age and neurodevelopmental disorders.</a>\n                </h2>\n  \n                \n                    <p class=\"categories-list\">\n                        \n                            <span class=\"label label-primary\">Journal article</span>\n                        \n                    </p>\n                \n\n                \n                \n                        \n                    <p itemprop=\"description\">Goriely A. et al, (2013), Am J Psychiatry, 170, 599 - 608</p>\n                \n                        \n                \n                    <p>\n                        \n                    </p>\n                \n                \n            </div>\n\n        </div>\n\n    </div>\n\n\n", 
        "\n\n    <div class=\"listing-item listing-item-publication\" itemscope itemprop=\"itemListElement\" itemtype=\"http://schema.org/PublicationVolume\">\n\n        <div class=\"row\">\n\n            \n\n            <div class=\"col-xs-12\">\n                            \n                \n                    <div class=\"pull-right\">\n                        <div class=\"altmetric-embed\" data-badge-popover=\"top\" data-badge-type=\"donut\" data-doi=\"10.1002/ajmg.a.35842\" data-hide-no-mentions=\"true\" data-link-target=\"_blank\"></div>\n                    </div>\n                \n            \n                <h2 class=\"media-heading\">\n                    <a href=\"https://www.rdm.ox.ac.uk/publications/402717\" title=\"The fibroblast growth factor receptor 2 p.Ala172Phe mutation in Pfeiffer syndrome--history repeating itself.\" data-toggle=\"modal\" data-target=\"#modal\" itemprop=\"name\" data-href=\"https://www.rdm.ox.ac.uk/publications/402717/@@modal\" class=\"state-synced\">The fibroblast growth factor receptor 2 p.Ala172Phe mutation in Pfeiffer syndrome--history repeating itself.</a>\n                </h2>\n  \n                \n                    <p class=\"categories-list\">\n                        \n                            <span class=\"label label-primary\">Journal article</span>\n                        \n                    </p>\n                \n\n                \n                \n                        \n                    <p itemprop=\"description\">Jay S. et al, (2013), Am J Med Genet A, 161A, 1158 - 1163</p>\n                \n                        \n                \n                    <p>\n                        \n                    </p>\n                \n                \n            </div>\n\n        </div>\n\n    </div>\n\n\n", 
        "\n\n    <div class=\"listing-item listing-item-publication\" itemscope itemprop=\"itemListElement\" itemtype=\"http://schema.org/PublicationVolume\">\n\n        <div class=\"row\">\n\n            \n\n            <div class=\"col-xs-12\">\n                            \n                \n                    <div class=\"pull-right\">\n                        <div class=\"altmetric-embed\" data-badge-popover=\"top\" data-badge-type=\"donut\" data-doi=\"10.1093/hmg/ddt015\" data-hide-no-mentions=\"true\" data-link-target=\"_blank\"></div>\n                    </div>\n                \n            \n                <h2 class=\"media-heading\">\n                    <a href=\"https://www.rdm.ox.ac.uk/publications/375700\" title=\"Cellular interference in craniofrontonasal syndrome: males mosaic for mutations in the X-linked EFNB1 gene are more severely affected than true hemizygotes.\" data-toggle=\"modal\" data-target=\"#modal\" itemprop=\"name\" data-href=\"https://www.rdm.ox.ac.uk/publications/375700/@@modal\" class=\"state-synced\">Cellular interference in craniofrontonasal syndrome: males mosaic for mutations in the X-linked EFNB1 gene are more severely affected than true hemizygotes.</a>\n                </h2>\n  \n                \n                    <p class=\"categories-list\">\n                        \n                            <span class=\"label label-primary\">Journal article</span>\n                        \n                    </p>\n                \n\n                \n                \n                        \n                    <p itemprop=\"description\">Twigg SRF. et al, (2013), Hum Mol Genet, 22, 1654 - 1662</p>\n                \n                        \n                \n                    <p>\n                        \n                    </p>\n                \n                \n            </div>\n\n        </div>\n\n    </div>\n\n\n", 
        "\n\n    <div class=\"listing-item listing-item-publication\" itemscope itemprop=\"itemListElement\" itemtype=\"http://schema.org/PublicationVolume\">\n\n        <div class=\"row\">\n\n            \n\n            <div class=\"col-xs-12\">\n                            \n                \n                    <div class=\"pull-right\">\n                        <div class=\"altmetric-embed\" data-badge-popover=\"top\" data-badge-type=\"donut\" data-doi=\"10.1093/brain/awt010\" data-hide-no-mentions=\"true\" data-link-target=\"_blank\"></div>\n                    </div>\n                \n            \n                <h2 class=\"media-heading\">\n                    <a href=\"https://www.rdm.ox.ac.uk/publications/384120\" title=\"Congenital myasthenic syndromes due to mutations in ALG2 and ALG14.\" data-toggle=\"modal\" data-target=\"#modal\" itemprop=\"name\" data-href=\"https://www.rdm.ox.ac.uk/publications/384120/@@modal\" class=\"state-synced\">Congenital myasthenic syndromes due to mutations in ALG2 and ALG14.</a>\n                </h2>\n  \n                \n                    <p class=\"categories-list\">\n                        \n                            <span class=\"label label-primary\">Journal article</span>\n                        \n                    </p>\n                \n\n                \n                \n                        \n                    <p itemprop=\"description\">Cossins J. et al, (2013), Brain, 136, 944 - 956</p>\n                \n                        \n                \n                    <p>\n                        \n                    </p>\n                \n                \n            </div>\n\n        </div>\n\n    </div>\n\n\n", 
        "\n\n    <div class=\"listing-item listing-item-publication\" itemscope itemprop=\"itemListElement\" itemtype=\"http://schema.org/PublicationVolume\">\n\n        <div class=\"row\">\n\n            \n\n            <div class=\"col-xs-12\">\n                            \n                \n                    <div class=\"pull-right\">\n                        <div class=\"altmetric-embed\" data-badge-popover=\"top\" data-badge-type=\"donut\" data-doi=\"10.1016/j.jpeds.2012.08.042\" data-hide-no-mentions=\"true\" data-link-target=\"_blank\"></div>\n                    </div>\n                \n            \n                <h2 class=\"media-heading\">\n                    <a href=\"https://www.rdm.ox.ac.uk/publications/356236\" title=\"Homozygous SALL1 mutation causes a novel multiple congenital anomaly-mental retardation syndrome.\" data-toggle=\"modal\" data-target=\"#modal\" itemprop=\"name\" data-href=\"https://www.rdm.ox.ac.uk/publications/356236/@@modal\" class=\"state-synced\">Homozygous SALL1 mutation causes a novel multiple congenital anomaly-mental retardation syndrome.</a>\n                </h2>\n  \n                \n                    <p class=\"categories-list\">\n                        \n                            <span class=\"label label-primary\">Journal article</span>\n                        \n                    </p>\n                \n\n                \n                \n                        \n                    <p itemprop=\"description\">Vodopiutz J. et al, (2013), J Pediatr, 162, 612 - 617</p>\n                \n                        \n                \n                    <p>\n                        \n                    </p>\n                \n                \n            </div>\n\n        </div>\n\n    </div>\n\n\n", 
        "\n\n    <div class=\"listing-item listing-item-publication\" itemscope itemprop=\"itemListElement\" itemtype=\"http://schema.org/PublicationVolume\">\n\n        <div class=\"row\">\n\n            \n\n            <div class=\"col-xs-12\">\n                            \n                \n                    <div class=\"pull-right\">\n                        <div class=\"altmetric-embed\" data-badge-popover=\"top\" data-badge-type=\"donut\" data-doi=\"10.1016/j.jpeds.2012.08.042\" data-hide-no-mentions=\"true\" data-link-target=\"_blank\"></div>\n                    </div>\n                \n            \n                <h2 class=\"media-heading\">\n                    <a href=\"https://www.rdm.ox.ac.uk/publications/389463\" title=\"Homozygous SALL1 mutation causes a novel multiple congenital anomaly - Mental retardation syndrome\" data-toggle=\"modal\" data-target=\"#modal\" itemprop=\"name\" data-href=\"https://www.rdm.ox.ac.uk/publications/389463/@@modal\" class=\"state-synced\">Homozygous SALL1 mutation causes a novel multiple congenital anomaly - Mental retardation syndrome</a>\n                </h2>\n  \n                \n                    <p class=\"categories-list\">\n                        \n                            <span class=\"label label-primary\">Journal article</span>\n                        \n                    </p>\n                \n\n                \n                \n                        \n                    <p itemprop=\"description\">Vodopiutz J. et al, (2013), Journal of Pediatrics, 162, 612 - 617</p>\n                \n                        \n                \n                    <p>\n                        \n                    </p>\n                \n                \n            </div>\n\n        </div>\n\n    </div>\n\n\n", 
        "\n\n    <div class=\"listing-item listing-item-publication\" itemscope itemprop=\"itemListElement\" itemtype=\"http://schema.org/PublicationVolume\">\n\n        <div class=\"row\">\n\n            \n\n            <div class=\"col-xs-12\">\n                            \n                \n                    <div class=\"pull-right\">\n                        <div class=\"altmetric-embed\" data-badge-popover=\"top\" data-badge-type=\"donut\" data-doi=\"10.1038/ng.2531\" data-hide-no-mentions=\"true\" data-link-target=\"_blank\"></div>\n                    </div>\n                \n            \n                <h2 class=\"media-heading\">\n                    <a href=\"https://www.rdm.ox.ac.uk/publications/375666\" title=\"Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis.\" data-toggle=\"modal\" data-target=\"#modal\" itemprop=\"name\" data-href=\"https://www.rdm.ox.ac.uk/publications/375666/@@modal\" class=\"state-synced\">Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis.</a>\n                </h2>\n  \n                \n                    <p class=\"categories-list\">\n                        \n                            <span class=\"label label-primary\">Journal article</span>\n                        \n                    </p>\n                \n\n                \n                \n                        \n                    <p itemprop=\"description\">Sharma VP. et al, (2013), Nat Genet, 45, 304 - 307</p>\n                \n                        \n                \n                    <p>\n                        \n                    </p>\n                \n                \n            </div>\n\n        </div>\n\n    </div>\n\n\n", 
        "\n\n    <div class=\"listing-item listing-item-publication\" itemscope itemprop=\"itemListElement\" itemtype=\"http://schema.org/PublicationVolume\">\n\n        <div class=\"row\">\n\n            \n\n            <div class=\"col-xs-12\">\n                            \n                \n                    <div class=\"pull-right\">\n                        <div class=\"altmetric-embed\" data-badge-popover=\"top\" data-badge-type=\"donut\" data-doi=\"10.1038/ejhg.2012.172\" data-hide-no-mentions=\"true\" data-link-target=\"_blank\"></div>\n                    </div>\n                \n            \n                <h2 class=\"media-heading\">\n                    <a href=\"https://www.rdm.ox.ac.uk/publications/350502\" title=\"Next-generation sequencing (NGS) as a diagnostic tool for retinal degeneration reveals a much higher detection rate in early-onset disease.\" data-toggle=\"modal\" data-target=\"#modal\" itemprop=\"name\" data-href=\"https://www.rdm.ox.ac.uk/publications/350502/@@modal\" class=\"state-synced\">Next-generation sequencing (NGS) as a diagnostic tool for retinal degeneration reveals a much higher detection rate in early-onset disease.</a>\n                </h2>\n  \n                \n                    <p class=\"categories-list\">\n                        \n                            <span class=\"label label-primary\">Journal article</span>\n                        \n                    </p>\n                \n\n                \n                \n                        \n                    <p itemprop=\"description\">Shanks ME. et al, (2013), Eur J Hum Genet, 21, 274 - 280</p>\n                \n                        \n                \n                    <p>\n                        \n                    </p>\n                \n                \n            </div>\n\n        </div>\n\n    </div>\n\n\n", 
        "\n\n    <div class=\"listing-item listing-item-publication\" itemscope itemprop=\"itemListElement\" itemtype=\"http://schema.org/PublicationVolume\">\n\n        <div class=\"row\">\n\n            \n\n            <div class=\"col-xs-12\">\n                            \n                \n                    <div class=\"pull-right\">\n                        <div class=\"altmetric-embed\" data-badge-popover=\"top\" data-badge-type=\"donut\" data-doi=\"10.1038/ng.2539\" data-hide-no-mentions=\"true\" data-link-target=\"_blank\"></div>\n                    </div>\n                \n            \n                <h2 class=\"media-heading\">\n                    <a href=\"https://www.rdm.ox.ac.uk/publications/375699\" title=\"Reduced dosage of ERF causes complex craniosynostosis in humans and mice and links ERK1/2 signaling to regulation of osteogenesis.\" data-toggle=\"modal\" data-target=\"#modal\" itemprop=\"name\" data-href=\"https://www.rdm.ox.ac.uk/publications/375699/@@modal\" class=\"state-synced\">Reduced dosage of ERF causes complex craniosynostosis in humans and mice and links ERK1/2 signaling to regulation of osteogenesis.</a>\n                </h2>\n  \n                \n                    <p class=\"categories-list\">\n                        \n                            <span class=\"label label-primary\">Journal article</span>\n                        \n                    </p>\n                \n\n                \n                \n                        \n                    <p itemprop=\"description\">Twigg SRF. et al, (2013), Nat Genet, 45, 308 - 313</p>\n                \n                        \n                \n                    <p>\n                        \n                    </p>\n                \n                \n            </div>\n\n        </div>\n\n    </div>\n\n\n", 
        "\n\n    <div class=\"listing-item listing-item-publication\" itemscope itemprop=\"itemListElement\" itemtype=\"http://schema.org/PublicationVolume\">\n\n        <div class=\"row\">\n\n            \n\n            <div class=\"col-xs-12\">\n                            \n                \n                    <div class=\"pull-right\">\n                        <div class=\"altmetric-embed\" data-badge-popover=\"top\" data-badge-type=\"donut\" data-doi=\"10.1038/ng.2539\" data-hide-no-mentions=\"true\" data-link-target=\"_blank\"></div>\n                    </div>\n                \n            \n                <h2 class=\"media-heading\">\n                    <a href=\"https://www.rdm.ox.ac.uk/publications/389189\" title=\"Reduced dosage of ERF causes complex craniosynostosis in humans and mice and links ERK1/2 signaling to regulation of osteogenesis\" data-toggle=\"modal\" data-target=\"#modal\" itemprop=\"name\" data-href=\"https://www.rdm.ox.ac.uk/publications/389189/@@modal\" class=\"state-synced\">Reduced dosage of ERF causes complex craniosynostosis in humans and mice and links ERK1/2 signaling to regulation of osteogenesis</a>\n                </h2>\n  \n                \n                    <p class=\"categories-list\">\n                        \n                            <span class=\"label label-primary\">Journal article</span>\n                        \n                    </p>\n                \n\n                \n                \n                        \n                    <p itemprop=\"description\">Twigg SRF. et al, (2013), Nature Genetics, 45, 308 - 313</p>\n                \n                        \n                \n                    <p>\n                        \n                    </p>\n                \n                \n            </div>\n\n        </div>\n\n    </div>\n\n\n"
    ], 
    "more": "\n\n    \n        <a href=\"https://www.rdm.ox.ac.uk/publications?random=2802f763-bf4d-412c-a247-ab18b3b2f53e&amp;b_start:int=100&amp;author=andrew-wilkie&amp;format=json\" title=\"Load more\" class=\"btn btn-default load-more-button\">\n            Load More\n        </a>\n    \n\n", 
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}