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American Journal of Human Genetics|January 13, 2000
Recombinational and mutational hotspots within the human lipoprotein lipase geneA R Templeton, A G Clark, K M Weiss, et al.American Journal of Human Genetics|January 13, 2000
NF1 microdeletion syndrome: refined FISH characterization of sporadic and familial deletions with locus-specific probesP Riva, L Corrado, F Natacci, et al.American Journal of Human Genetics|January 13, 2000
Full-genome scan for linkage in 50 families segregating the bipolar affective disease phenotypeC Friddle, R Koskela, K Ranade, et al.American Journal of Human Genetics|February 1, 1994
Detection of a major gene for heterocellular hereditary persistence of fetal hemoglobin after accounting for genetic modifiersS L Thein, M Sampietro, K Rohde, et al.American Journal of Human Genetics|March 1, 1994
Genetic analysis of Hispanic individuals with cystic fibrosisT A Grebe, W K Seltzer, J DeMarchi, et al.American Journal of Human Genetics|January 1, 1995
Is congenital bilateral absence of vas deferens a primary form of cystic fibrosis? Analyses of the CFTR gene in 67 patientsB Mercier, C Verlingue, W Lissens, et al.American Journal of Human Genetics|November 1, 1995
Mutation T318M in the CYP11B2 gene encoding P450c11AS (aldosterone synthase) causes corticosterone methyl oxidase II deficiencyG Zhang, H Rodriguez, C E Fardella, et al.American Journal of Human Genetics|November 1, 1995
Molecular analysis of 24 Alagille syndrome families identifies a single submicroscopic deletion and further localizes the Alagille region within 20p12E B Rand, N B Spinner, D A Piccoli, et al.American Journal of Human Genetics|November 1, 1995
A gene that regulates DNA replication in response to DNA damage is located on human chromosome 4qG W Verhaegh, W Jongmans, N G Jaspers, et al.American Journal of Human Genetics|November 1, 1995
Sex chromosome loss and aging: in situ hybridization studies on human interphase nucleiM Guttenbach, B Koschorz, U Bernthaler, et al.Pageof 979