[Fragile X syndrome: epidemiology, genetics, diagnosis]
Rev Prat
.
2001 Sep 1;51(13):1477-80.
[Article in French]
Authors
P Beauvais
1
,
C Houdayer
Affiliation
1
Service de neuropédiatrie, hôpital Trousseau, 75571 Paris.
PMID:
11601079
No abstract available
Publication types
Comparative Study
Review
MeSH terms
Cytogenetics
Diagnosis, Differential
Female
Fragile X Syndrome* / diagnosis
Fragile X Syndrome* / epidemiology
Fragile X Syndrome* / genetics
Genetic Techniques
Humans
Male
Mutation
Pedigree
Sex Factors