000 01431 a2200481 4500
005 20250515160438.0
264 0 _c20090313
008 200903s 0 0 fre d
022 _a0041-4131
040 _aNLM
_beng
_cNLM
100 1 _aBen Jemaa, Lamia
245 0 0 _a[Molecular diagnosis of fragile X syndrome].
_h[electronic resource]
260 _bLa Tunisie medicale
_cNov 2008
300 _a973-7 p.
_bdigital
500 _aPublication Type: English Abstract; Journal Article
650 0 4 _aAbnormalities, Multiple
_xgenetics
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aCraniofacial Abnormalities
_xgenetics
650 0 4 _aFragile X Mental Retardation Protein
_xgenetics
650 0 4 _aFragile X Syndrome
_xdiagnosis
650 0 4 _aGenetic Counseling
650 0 4 _aGenetic Markers
650 0 4 _aGenetic Testing
650 0 4 _aHumans
650 0 4 _aIntellectual Disability
_xgenetics
650 0 4 _aMale
650 0 4 _aMutation
650 0 4 _aPedigree
650 0 4 _aPuberty
650 0 4 _aRetrospective Studies
650 0 4 _aTestis
_xabnormalities
650 0 4 _aTunisia
700 1 _aKhemir, Samah
700 1 _aMaazoul, Faouzi
700 1 _aRichard, Laurent
700 1 _aBeldjord, Cherif
700 1 _aChaabouni, Myriam
700 1 _aChaabouni, Habiba
773 0 _tLa Tunisie medicale
_gvol. 86
_gno. 11
_gp. 973-7
999 _c18656923
_d18656923