000 01334 a2200385 4500
005 20250513133458.0
264 0 _c19980219
008 199802s 0 0 eng d
022 _a0741-0395
024 7 _a10.1002/(SICI)1098-2272(1997)14:6<1113::AID-GEPI92>3.0.CO;2-J
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aSchaid, D J
245 0 0 _aGenotype relative-risks and association tests for nuclear families with missing parental data.
_h[electronic resource]
260 _bGenetic epidemiology
_c1997
300 _a1113-8 p.
_bdigital
500 _aPublication Type: Clinical Trial; Journal Article; Randomized Controlled Trial; Research Support, U.S. Gov't, P.H.S.
650 0 4 _aAlgorithms
650 0 4 _aAlleles
650 0 4 _aFemale
650 0 4 _aGenetic Diseases, Inborn
_xgenetics
650 0 4 _aGenetic Markers
650 0 4 _aGenotype
650 0 4 _aHumans
650 0 4 _aLikelihood Functions
650 0 4 _aLinkage Disequilibrium
650 0 4 _aMale
650 0 4 _aNuclear Family
650 0 4 _aParents
650 0 4 _aPhenotype
650 0 4 _aProbability
650 0 4 _aRisk Factors
700 1 _aLi, H
773 0 _tGenetic epidemiology
_gvol. 14
_gno. 6
_gp. 1113-8
856 4 0 _uhttps://doi.org/10.1002/(SICI)1098-2272(1997)14:6<1113::AID-GEPI92>3.0.CO;2-J
_zAvailable from publisher's website
999 _c9403006
_d9403006