TY  - GEN
AU  - Ben Jemaa,Lamia
AU  - Khemir,Samah
AU  - Maazoul,Faouzi
AU  - Richard,Laurent
AU  - Beldjord,Cherif
AU  - Chaabouni,Myriam
AU  - Chaabouni,Habiba
TI  - [Molecular diagnosis of fragile X syndrome]
SN  - 0041-4131
PY  - 2009///0313
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Adolescent
KW  - Adult
KW  - Child
KW  - Child, Preschool
KW  - Craniofacial Abnormalities
KW  - Fragile X Mental Retardation Protein
KW  - Fragile X Syndrome
KW  - diagnosis
KW  - Genetic Counseling
KW  - Genetic Markers
KW  - Genetic Testing
KW  - Humans
KW  - Intellectual Disability
KW  - Male
KW  - Mutation
KW  - Pedigree
KW  - Puberty
KW  - Retrospective Studies
KW  - Testis
KW  - abnormalities
KW  - Tunisia
N1  - Publication Type: English Abstract; Journal Article
ER  -