A syndrome of deaf-mutism associated with albinism showing dominant autosomal inheritance
Am J Hum Genet
.
1963 Sep;15(3):259-64.
Author
W TIETZ
PMID:
13985019
PMCID:
PMC1932384
No abstract available
MeSH terms
Albinism*
Deafness*
Eyebrows*
Heredity*
Humans
Pigmentation*
Syndrome*