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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