000 01463 a2200421 4500
005 20250514200055.0
264 0 _c20050318
008 200503s 0 0 eng d
022 _a1552-4825
024 7 _a10.1002/ajmg.a.30237
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aBiancalana, Valérie
245 0 0 _aFive years of molecular diagnosis of Fragile X syndrome (1997-2001): a collaborative study reporting 95% of the activity in France.
_h[electronic resource]
260 _bAmerican journal of medical genetics. Part A
_cSep 2004
300 _a218-24 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAge Factors
650 0 4 _aBlotting, Southern
650 0 4 _aChild
650 0 4 _aFemale
650 0 4 _aFragile X Syndrome
_xgenetics
650 0 4 _aFrance
650 0 4 _aGenetic Testing
_xmethods
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aPolymerase Chain Reaction
650 0 4 _aSensitivity and Specificity
650 0 4 _aSex Factors
700 1 _aBeldjord, Chérif
700 1 _aTaillandier, Agnès
700 1 _aSzpiro-Tapia, Sylvie
700 1 _aCusin, Véronica
700 1 _aGerson, Fabienne
700 1 _aPhilippe, Christophe
700 1 _aMandel, Jean-Louis
773 0 _tAmerican journal of medical genetics. Part A
_gvol. 129A
_gno. 3
_gp. 218-24
856 4 0 _uhttps://doi.org/10.1002/ajmg.a.30237
_zAvailable from publisher's website
999 _c15024487
_d15024487