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Journal of Medical Genetics|January 20, 2017

Delineating the phenotypic spectrum of Bainbridge-Ropers syndrome: 12 new patients with <i>de novo</i>, heterozygous, loss-of-function mutations in <i>ASXL3</i> and review of published literatureM Balasubramanian, J Willoughby, A E Fry, et al.

Journal of Medical Genetics|July 17, 2008

Clinical and molecular delineation of the 17q21.31 microdeletion syndromeD A Koolen, A J Sharp, J A Hurst, et al.

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Search research articles

Showing results (11-20 of 12) with videos related to

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Journal of Medical Genetics|January 20, 2017

Delineating the phenotypic spectrum of Bainbridge-Ropers syndrome: 12 new patients with <i>de novo</i>, heterozygous, loss-of-function mutations in <i>ASXL3</i> and review of published literatureM Balasubramanian, J Willoughby, A E Fry, et al.

Journal of Medical Genetics|July 17, 2008

Clinical and molecular delineation of the 17q21.31 microdeletion syndromeD A Koolen, A J Sharp, J A Hurst, et al.

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