[Rothmund's syndrome: observations in one case]
J Genet Hum
.
1976 Nov:24 Suppl:151-64.
[Article in French]
Authors
A Ourgaud
,
H Payan
,
F Giraud
,
J F Mattei
,
J M Merlihot
,
P Pommier de Santi
PMID:
1025264
No abstract available
Publication types
Case Reports
MeSH terms
Adolescent
Cataract / genetics*
Diagnosis, Differential
Humans
Male
Phenotype
Rothmund-Thomson Syndrome / genetics*
Skin / pathology
Skin Diseases / genetics*