Pendred syndrome
J Med Genet
.
1996 Dec;33(12):1037-40.
doi: 10.1136/jmg.33.12.1037.
Authors
W Reardon
1
,
R C Trembath
Affiliation
1
Mothercare Unit of Paediatric Genetics and Fetal Medicine, Institute of Child Health, London, UK.
PMID:
9004139
PMCID:
PMC1050818
DOI:
10.1136/jmg.33.12.1037
No abstract available
Publication types
Research Support, Non-U.S. Gov't
Review
MeSH terms
Chromosomes, Human, Pair 7 / genetics
Deafness*
Female
Humans
Male
Syndrome
Thyroid Gland / physiopathology