Showing results (2911-2920 of 9,807) with videos related to
Sort By:
Pageof 981
American Journal of Human Genetics|September 1, 1994
Multipoint linkage map of the human pseudoautosomal region, based on single-sperm typing: do double crossovers occur during male meiosis?K Schmitt, L C Lazzeroni, S Foote, et al.American Journal of Human Genetics|March 1, 1991
Prenatal screening for hemoglobinopathies. III. Applicability of the health belief modelP T Rowley, S Loader, C J Sutera, et al.American Journal of Human Genetics|March 1, 1991
Thermolabile methylenetetrahydrofolate reductase: an inherited risk factor for coronary artery diseaseS S Kang, P W Wong, A Susmano, et al.American Journal of Human Genetics|March 1, 1991
Intermediate hyperhomocysteinemia resulting from compound heterozygosity of methylenetetrahydrofolate reductase mutationsS S Kang, P W Wong, H G Bock, et al.American Journal of Human Genetics|March 1, 1991
A mutation in the second nucleotide binding fold of the cystic fibrosis geneL Osborne, R Knight, G Santis, et al.American Journal of Human Genetics|March 1, 1991
Identification of a novel phenylketonuria (PKU) mutation in the Chinese: further evidence for multiple origins of PKU in AsiaT Wang, Y Okano, R C Eisensmith, et al.American Journal of Human Genetics|December 1, 2009
A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depressionHelen M Knight, Benjamin S Pickard, Alan Maclean, et al.American Journal of Human Genetics|December 1, 2009
Short telomeres are sufficient to cause the degenerative defects associated with agingMary Armanios, Jonathan K Alder, Erin M Parry, et al.American Journal of Human Genetics|December 1, 2009
Genomic dissection of population substructure of Han Chinese and its implication in association studiesShuhua Xu, Xianyong Yin, Shilin Li, et al.American Journal of Human Genetics|February 1, 1991
Two frameshift mutations in the cystic fibrosis geneM C Iannuzzi, R C Stern, F S Collins, et al.Pageof 981