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Autosomal dominant nonsyndromic hearing loss 5
- ... mutations is the most identified subtype of nonsyndromic autosomal dominant ... Mol Med. 2009 Jun;9(5):546-64. doi: 10.2174/156652409788488775. Citation on ...
- ... type 4 Genetic Testing Registry: Stickler syndrome, type 5 Stickler ... STL2 STICKLER SYNDROME, TYPE I, NONSYNDROMIC OCULAR STICKLER SYNDROME, TYPE V; STL5 STICKLER SYNDROME, ...
- ... should. FGFR3 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. FGFR3-associated coronal synostosis Muenke nonsyndromic coronal craniosynostosis Genetic Testing Registry: Muenke syndrome Muenke ...