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Behavior Genetics|May 1, 1977
Assortative marriage for cognitive abilitiesA B Zonderman, S G Vandenberg, K P Spuhler, et al.Medical Hypotheses|August 1, 1981
Sex differences in lung cancer incidence: a genetic modelP R Fain, H T Lynch, W A Albano, et al.Human Molecular Genetics|June 1, 1996
Comparison of BRCA1 polymorphisms, rare sequence variants and/or missense mutations in unaffected and breast/ovarian cancer populationsF Durocher, D Shattuck-Eidens, M McClure, et al.Hereditary Cancer in Clinical Practice|May 3, 2016
Assessing biases of information contained in pedigrees for the classification of BRCA-genetic variants: a study arising from the ENIGMA analytical working groupC H H Kerkhofs, A B Spurdle, P J Lindsey, et al.Human Molecular Genetics|October 1, 1996
A high resolution CEPH crossover mapping panel and integrated map of chromosome 11P R Fain, E N Kort, C Yousry, et al.American Journal of Human Genetics|January 1, 1989
The order of loci in the pericentric region of chromosome 17, based on evidence from physical and genetic breakpointsP R Fain, E Wright, H F Willard, et al.Journal of the National Cancer Institute|December 4, 1991
Inheritance of nevus number and size in melanoma and dysplastic nevus syndrome kindredsD E Goldgar, L A Cannon-Albright, L J Meyer, et al.Genomics|December 1, 1991
Localization of the highly polymorphic microsatellite DXS456 on the genetic linkage map of the human X chromosomeP R Fain, J A Luty, Z Guo, et al.Neurology|April 1, 1996
Refined genetic mapping and proteolipid protein mutation analysis in X-linked pure hereditary spastic paraplegiaF Cambi, X M Tang, P Cordray, et al.The New England Journal of Medicine|October 6, 1988
Linkage heterogeneity of autosomal dominant polycystic kidney diseaseW J Kimberling, P R Fain, J B Kenyon, et al.Pageof 10