White forelock, pigmentary disorder of irides, and long segment Hirschsprung disease: Possible variant of Waardenburg syndrome

Mendelian Inheritance in Man. Catalogs of Autosomal Dominant, Autosomal Recessive, and X-Linked Phenotypes.

1967 • 1,002 citations

Recognizable Patterns of Human Malformation

1985 • 922 citations

A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root with pigmentary defects of the iris and head hair and with congenital deafness.

1951 • 627 citations

Heterogeneity in Waardenburg syndrome.

1977 • 116 citations

Waardenburg's syndrome

1960 • 104 citations

The association of Waardenburg syndrome and Hirschsprung megacolon

1979 • 104 citations

Partial Albinism and Deaf Mutism

1962 • 98 citations

Failure of Rubella Herd Immunity during an Epidemic

1973 • 54 citations

Dominant piebald trait (white forelock and leukoderma) with neurological impairment.

1971 • 47 citations

STUDIES ON MEGACOLON IN PIEBALD MICE

1962 • 46 citations

Congenital Deafness and Hirschsprung’s Disease

1973 • 32 citations