WAARDENBURG SYNDROME, TYPE 1; WS1

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Summary

Literature (2)

Literature for OMIM 193500: WAARDENBURG SYNDROME, TYPE 1; WS1

Xenbase Articles:
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Denotes literature images)

Systematic discovery of nonobvious human disease models through orthologous phenotypes., McGary KL,Park TJ,Woods JO,Cha HJ,Wallingford JB,Marcotte EM, Proc Natl Acad Sci U S A. April 6, 2010; 107(14):1091-6490.
Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes., Neal SJ,Rajasekaran A,Jusić N,Taylor L,Read M,Alfandari D,Alfandari D,Pignoni F,Moody SA, J Exp Zool B Mol Dev Evol. May 1, 2024; 342(3):1552-5015.

Systematic discovery of nonobvious human disease models through orthologous phenotypes., McGary KL,Park TJ,Woods JO,Cha HJ,Wallingford JB,Marcotte EM, Proc Natl Acad Sci U S A. April 6, 2010; 107(14):1091-6490.

Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes., Neal SJ,Rajasekaran A,Jusić N,Taylor L,Read M,Alfandari D,Alfandari D,Pignoni F,Moody SA, J Exp Zool B Mol Dev Evol. May 1, 2024; 342(3):1552-5015.