All individuals with variants in gene ZEB2

10 entries on 1 page. Showing entries 1 - 10.
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00000029 - PubMed: Almomani 2011 - - - - - - 0 - - - - 1 1 LOVD-team, but with Curator vacancy
00037447 - - - - - Germany - - 0 - - - - 1 1 Andreas Laner
00037448 - - - - - Germany - - 0 - - myopathy, mitochondrial Mowat-Wilson syndrome 1 1 Andreas Laner
00037449 - - - - - Germany - - 0 - - ? CGH-array complex dysmorphy, kraniofaziale Dysmorphie, verstrichenes Philtrum, wide thumbs, Fingerpads, lange dichte Wimpern, Scapulae alatae, Enkopresis 1 1 Andreas Laner
00037450 - - - - - Germany - - 0 - - ? developmental delay 1 1 Andreas Laner
00081000 - Trujillano et al., submitted unaffected non-carrier parents - - - - - 0 - - MOWS Mowat-Wilson syndrome (OMIM:235730) 1 1 Daniel Trujillano
00102081 P10 - - F no China - >08y - - - ID HP:0000252; HP:0001999; HP:0001250; HP:0007364; intellectual disability (HP:0001249) 1 1 Wenjuan Qiu
00133267 HK164C - - M - Hong Kong - - 0 - - HCAD - 1 1 Xuehan Zhuang
00150166 26539891-FamBAB3413 PubMed: Karaca 2015 - - - - - - 0 family structure in paper - ? intellectual diability, CCA, severe intellectual diability, epilepsy, no ambulation, pointed chin, cupped ears 1 1 Johan den Dunnen
00292250 - Faruq 2020, submitted analysis 2794 individuals (India) - - India - - 0 - - ? - 1 1 Mohammed Faruq
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