All individuals with variants in gene SIX5

10 entries on 1 page. Showing entries 1 - 10.
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00132985 29100090-FamDC7 PubMed: Sanna-Cherchi 2017, Journal: Sanna-Cherchi 2017 2-genertion family, heterozygous carrier mother M - - - - - - - CAKUT CAKUT, renal dysplasia left 1 2 Johan den Dunnen
00285358 - PubMed: Hwang 2014 - - - - - - - - - ? - 1 1 Global Variome, with Curator vacancy
00285359 - PubMed: Hoskins 2007, PubMed: Smith 1993, PubMed: Krug 2011, PubMed: Hwang 2014 - - - - - - - - - ? - 1 1 Global Variome, with Curator vacancy
00285360 - PubMed: Hoskins 2007, PubMed: Smith 1993 - - - - - - - - - ? - 1 1 Global Variome, with Curator vacancy
00285361 - PubMed: Hoskins 2007, PubMed: Smith 1993 - - - - - - - - - ? - 1 1 Global Variome, with Curator vacancy
00285362 - PubMed: Hoskins 2007, PubMed: Smith 1993 - - - - - - - - - ? - 1 1 Global Variome, with Curator vacancy
00316147 K29 PubMed: Heidet 2017 fetus - - France - - - - - CAKUT bilateral kidney agenesis 1 1 Johan den Dunnen
00324401 Pat2 PubMed: Barrie 2019 2-generation family, 1 affected, unaffected heterozygous carrier parents M - United States - - - - - ? see paper; ..., typical facial features, microcephaly, wide nasal bridge; intrauterine/postnatal growth retardation; intellectual disability/developmental delay; hypotonia; no seizuresĀ and/or distinctive EEG abnormalities; feeding difficulties; skin changes (hemangioma; marble/dry skin); no antibody deficiency; genitourinary tract anomalies; no structural brain anomalies 1 1 Johan den Dunnen
00384520 - - - M yes Saudi Arabia - - - - - deafness nonsyndromic deafness 1 1 Muhammad Umair
00465470 - PubMed: Wu 2019 analysis 1291 cases hearing loss - - Taiwan - - - - - HL - 1 1 Johan den Dunnen
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