000 01177 a2200337 4500
005 20250515072132.0
264 0 _c20070904
008 200709s 0 0 eng d
022 _a0002-9297
024 7 _a10.1086/518670
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aShi, Min
245 0 0 _aIdentification of risk-related haplotypes with the use of multiple SNPs from nuclear families.
_h[electronic resource]
260 _bAmerican journal of human genetics
_cJul 2007
300 _a53-66 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, N.I.H., Intramural
650 0 4 _aFemale
650 0 4 _aGenetic Markers
_xgenetics
650 0 4 _aGenetic Predisposition to Disease
_xgenetics
650 0 4 _aGenetic Testing
_xmethods
650 0 4 _aHaplotypes
_xgenetics
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aNuclear Family
650 0 4 _aPolymorphism, Single Nucleotide
650 0 4 _aRisk
700 1 _aUmbach, David M
700 1 _aWeinberg, Clarice R
773 0 _tAmerican journal of human genetics
_gvol. 81
_gno. 1
_gp. 53-66
856 4 0 _uhttps://doi.org/10.1086/518670
_zAvailable from publisher's website
999 _c17103275
_d17103275