Bilateral complete radioulnar synostosis associated with ectrodactyly and sensorineural hearing loss: a variant of SHFM1.
作者信息
Debeer Ph, Vandenbossche L, de Ravel T J L, Desloovere C, De Smet L, Huysmans C, Thoelen R, Vermeesch J, Van de Ven W J M, Fryns J P
出版信息
Clin Genet. 2004 Feb;65(2):153-5. doi: 10.1111/j.0009-9163.2004.00202.x.
Abstract
摘要
Zotero 插件