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Human Genetics|June 1, 1990
The mutational spectrum of single base-pair substitutions causing human genetic disease: patterns and predictionsD N Cooper, M KrawczakHuman Genetics|August 6, 2011
Functional haplotypes of Fc gamma (Fcγ) receptor (FcγRIIA and FcγRIIIB) predict risk to repeated episodes of severe malarial anemia and mortality in Kenyan childrenCollins Ouma, Gregory C Davenport, Steven Garcia, et al.Human Genetics|June 1, 1990
The achondroplasia gene is not linked to the locus for neurofibromatosis 1 on chromosome 17S M Pulst, J M Graham, P Fain, et al.Human Genetics|May 20, 2011
Hyperuricemia cosegregating with osteogenesis imperfecta is associated with a mutation in GPATCH8Hiroshi Kaneko, Hiroshi Kitoh, Tohru Matsuura, et al.Human Genetics|June 7, 2011
Alterations of ATM and CADM1 in chromosomal 11q22.3-23.2 region are associated with the development of invasive cervical carcinomaDipanjana Mazumder Indra, Sraboni Mitra, Anup Roy, et al.Human Genetics|June 11, 2011
A scaffold for X chromosome inactivationAnna Tattermusch, Neil BrockdorffHuman Genetics|June 11, 2011
A signature of balancing selection in the region upstream to the human UGT2B4 gene and implications for breast cancer riskChang Sun, Dezheng Huo, Catherine Southard, et al.Human Genetics|June 15, 2011
The role of the TCF4 gene in the phenotype of individuals with 18q segmental deletionsMinire Hasi, Bridgette Soileau, Courtney Sebold, et al.Human Genetics|November 1, 1990
Selective advantage of fra (X) heterozygotesF Vogel, W E Crusio, C Kovac, et al.Pageof 959