000 01339 a2200373 4500
005 20250516054314.0
264 0 _c20120118
008 201201s 0 0 eng d
022 _a1552-4833
024 7 _a10.1002/ajmg.a.34195
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aDuclos, Aude
245 0 0 _aPitfalls in the use of DGV for CNV interpretation.
_h[electronic resource]
260 _bAmerican journal of medical genetics. Part A
_cOct 2011
300 _a2593-6 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aColorectal Neoplasms, Hereditary Nonpolyposis
_xgenetics
650 0 4 _aComparative Genomic Hybridization
_xmethods
650 0 4 _aDNA Copy Number Variations
_xgenetics
650 0 4 _aDatabases, Genetic
650 0 4 _aGenetics, Medical
_xmethods
650 0 4 _aGenomic Structural Variation
_xgenetics
650 0 4 _aHumans
650 0 4 _aResearch Design
700 1 _aCharbonnier, Françoise
700 1 _aChambon, Pascal
700 1 _aLatouche, Jean-Baptiste
700 1 _aBlavier, André
700 1 _aRedon, Richard
700 1 _aFrébourg, Thierry
700 1 _aFlaman, Jean-Michel
773 0 _tAmerican journal of medical genetics. Part A
_gvol. 155A
_gno. 10
_gp. 2593-6
856 4 0 _uhttps://doi.org/10.1002/ajmg.a.34195
_zAvailable from publisher's website
999 _c21150079
_d21150079