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[Craniofacial-deafness-hand syndrome].
Ryoikibetsu Shokogun Shirizu. 2001;(33):511-2.
Ryoikibetsu Shokogun Shirizu. 2001.
PMID: 11462543
Review.
Japanese.
No abstract available.
Pax genes in embryogenesis and oncogenesis.
Wang Q, Fang WH, Krupinski J, Kumar S, Slevin M, Kumar P.
Wang Q, et al.
J Cell Mol Med. 2008 Dec;12(6A):2281-94. doi: 10.1111/j.1582-4934.2008.00427.x. Epub 2008 Jul 4.
J Cell Mol Med. 2008.
PMID: 18627422
Free PMC article.
Review.
Mutation in PAX3 causes Waardenburg syndrome, and craniofacial-deafness-hand syndrome. The Splotch phenotype in mouse exhibits defects in neural crest derivatives such as, pigment cells, sympathetic ganglia and cardiac neural crest-derived structures. …
Mutation in PAX3 causes Waardenburg syndrome, and craniofacial-deafness-hand syndrome. The Splotch phenotype in …
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