waardenburg syndrome pedigree

Basic mendelian pedigree patterns.



Waardenburg syndrome is usually (Pedigree for williams syndrome >> pedigree



Pedigree structure and co-segregation of NPS in four families.



Pedigree showing incomplete penetrance for autosomal dominant disease.



Pedigrees of mitochondrial diseases.



Waardenburg syndrome is usually



Nonsense mutations in the PAX3 gene cause Waardenburg syndrome type I in two



and individuals with Waardenburg Syndrome may also be congenitally deaf.



Apparent Digenic Inheritance of Waardenburg Syndrome Type 2 (WS2) and



Waardenburg Syndrome, Type 2 | Hereditary Ocular Diseases



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