[Molecular analysis of 68 Swiss-Romance subjects at risk for fragile X syndrome]
Rev Med Suisse Romande
.
1993 Apr;113(4):309-11.
[Article in French]
Authors
D F Schorderet
1
,
F Thonney
,
N Pillet
,
C Delozier-Blanchet
,
P Marguerat
,
G Pescia
Affiliation
1
Division autonome de génétique médicale, CHUV, Lausanne.
PMID:
8502886
No abstract available
Publication types
Research Support, Non-U.S. Gov't
MeSH terms
Adult
Blotting, Southern
Child
Female
Fragile X Syndrome / genetics*
Gene Amplification
Heterozygote
Humans
Male
Mutation
Polymerase Chain Reaction*