000 01387 a2200469 4500
005 20250513045955.0
264 0 _c19950322
008 199503s 0 0 eng d
022 _a0148-7299
024 7 _a10.1002/ajmg.1320530413
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aPuissant, H
245 0 0 _aMolecular analysis of 53 fragile X families with the probe StB12.3.
_h[electronic resource]
260 _bAmerican journal of medical genetics
_cDec 1994
300 _a370-3 p.
_bdigital
500 _aPublication Type: Comparative Study; Journal Article
650 0 4 _aAlleles
650 0 4 _aDNA Probes
650 0 4 _aFamily Health
650 0 4 _aFemale
650 0 4 _aFragile X Syndrome
_xdiagnosis
650 0 4 _aGenetic Linkage
650 0 4 _aGenetic Markers
650 0 4 _aHeterozygote
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMutation
650 0 4 _aPedigree
650 0 4 _aPregnancy
650 0 4 _aPrenatal Diagnosis
700 1 _aMalinge, M C
700 1 _aLarget-Piet, A
700 1 _aMartin, D
700 1 _aChauveau, P
700 1 _aOdent, S
700 1 _aPlessis, G
700 1 _aParent, P
700 1 _aLemarec, B
700 1 _aLarget-Piet, L
773 0 _tAmerican journal of medical genetics
_gvol. 53
_gno. 4
_gp. 370-3
856 4 0 _uhttps://doi.org/10.1002/ajmg.1320530413
_zAvailable from publisher's website
999 _c7863383
_d7863383