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Literature for DOID 9258: Waardenburg syndrome
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.
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Modeling human congenital disorders with neural crest developmental defects using patient-derived induced pluripotent stem cells.,
Okuno H,Okano H,
Regen Ther. August 24, 2021; 18:2352-3204.
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Time-resolved quantitative proteomic analysis of the developing Xenopus otic vesicle reveals putative congenital hearing loss candidates.,
Baxi AB,Nemes P,Moody SA,
iScience. September 15, 2023; 26(9):2589-0042.
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