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[Craniofacial-deafness-hand syndrome].
Okuyama T. Okuyama T. 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 …