000 01378 a2200385 4500
005 20250514215427.0
264 0 _c20060420
008 200604s 0 0 eng d
022 _a1468-6244
024 7 _a10.1136/jmg.2004.025478
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aLe Caignec, C
245 0 0 _aDetection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformations.
_h[electronic resource]
260 _bJournal of medical genetics
_cFeb 2005
300 _a121-8 p.
_bdigital
500 _aPublication Type: Evaluation Study; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAbnormalities, Multiple
_xdiagnosis
650 0 4 _aChromosome Aberrations
650 0 4 _aFetus
_xabnormalities
650 0 4 _aGenomics
_xmethods
650 0 4 _aHumans
650 0 4 _aIn Situ Hybridization, Fluorescence
650 0 4 _aOligonucleotide Array Sequence Analysis
_xmethods
650 0 4 _aPhenotype
650 0 4 _aPrenatal Diagnosis
_xmethods
700 1 _aBoceno, M
700 1 _aSaugier-Veber, P
700 1 _aJacquemont, S
700 1 _aJoubert, M
700 1 _aDavid, A
700 1 _aFrebourg, T
700 1 _aRival, J M
773 0 _tJournal of medical genetics
_gvol. 42
_gno. 2
_gp. 121-8
856 4 0 _uhttps://doi.org/10.1136/jmg.2004.025478
_zAvailable from publisher's website
999 _c15366497
_d15366497