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Subject Developmental -- Clinical genetics -- Copy-number -- Diagnostics tests

1. Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin–Siris syndrome. Issue 3 (5th November 2015)

Authors:
Hempel, Annmarie; Pagnamenta, Alistair T; Blyth, Moira; Mansour, Sahar; McConnell, Vivienne; Kou, Ikuyo; Ikegawa, Shiro; Tsurusaki, Yoshinori; Matsumoto, Naomichi; Lo-Castro, Adriana; Plessis, Ghislaine; Albrecht, Beate; Battaglia, Agatino; Taylor, Jenny C; Howard, Malcolm F; Keays, David; Sohal,...
Journal:
Journal of medical genetics
Issue:
Volume 53:Issue 3(2016)
Page Start:
152
Record Type:
Journal Article
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