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Authors
Polla, D.L.
Bhoj, E.J.
Verheij, J.B.G.M.
Wassink-Ruiter, J.S. Klein
Reis, A.
Deshpande, C.
Gregor, A.
Hill-Karfe, K.
Silfhout, A.T. Vulto-van
Pfundt, R.
Bongers, E.M.H.F.
Hakonarson, H.
Berland, S.
Gradek, G.
Banka, S.
Chandler, K.
Gompertz, L.
Huffels, S.C.
Stumpel, C.T.R.M.
Wennekes, R.
Stegmann, A.P.A.
Reardon, W.
Leenders, E.K.S.M.
de Vries, B.B.A.
Li, D.
Zackai, E.
Ragge, N.
Lynch, S.A.
Cuddapah, S.
van Bokhoven, H.
Zweier, C.
de Brouwer, A.P.M. http://orcid.org/0000-0002-2131-0484
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This article is maintained by: Elsevier
Article Title: De novo variants in MED12 cause X-linked syndromic neurodevelopmental disorders in 18 females
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-020-01040-6
Content Type: article
Copyright: © 2021, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics
