Smith-Lemli-Opitz syndrome in an inbred family
Am J Dis Child
.
1972 Sep;124(3):431-3.
doi: 10.1001/archpedi.1972.02110150129021.
Authors
S Nevo
,
A Benderly
,
J Levy
,
M B Katznelson
PMID:
5056882
DOI:
10.1001/archpedi.1972.02110150129021
No abstract available
MeSH terms
Abnormalities, Multiple*
Adult
Consanguinity
Female
Growth Disorders*
Humans
Infant
Intellectual Disability*
Male
Microcephaly*
Syndrome