000 01491 a2200457 4500
005 20250516045936.0
264 0 _c20111209
008 201112s 0 0 eng d
022 _a1423-0062
024 7 _a10.1159/000324683
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aLin, Peng
245 0 0 _aCopy number variation accuracy in genome-wide association studies.
_h[electronic resource]
260 _bHuman heredity
_c2011
300 _a141-7 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, N.I.H., Extramural
650 0 4 _aDNA Copy Number Variations
_xgenetics
650 0 4 _aGenome-Wide Association Study
_xmethods
650 0 4 _aHumans
650 0 4 _aPolymorphism, Single Nucleotide
_xgenetics
650 0 4 _aPredictive Value of Tests
650 0 4 _aReproducibility of Results
650 0 4 _aSoftware
700 1 _aHartz, Sarah M
700 1 _aWang, Jen-Chyong
700 1 _aKrueger, Robert F
700 1 _aForoud, Tatiana M
700 1 _aEdenberg, Howard J
700 1 _aNurnberger, John I
700 1 _aBrooks, Andrew I
700 1 _aTischfield, Jay A
700 1 _aAlmasy, Laura
700 1 _aWebb, Bradley T
700 1 _aHesselbrock, Victor M
700 1 _aPorjesz, Bernice
700 1 _aGoate, Alison M
700 1 _aBierut, Laura J
700 1 _aRice, John P
773 0 _tHuman heredity
_gvol. 71
_gno. 3
_gp. 141-7
856 4 0 _uhttps://doi.org/10.1159/000324683
_zAvailable from publisher's website
999 _c21025695
_d21025695