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American Journal of Human Genetics|September 1, 1994
Molecular mapping of the Edwards syndrome phenotype to two noncontiguous regions on chromosome 18L Boghosian-Sell, R Mewar, W Harrison, et al.Genomics|April 10, 1995
Molecular cloning and characterization of the active human mitochondrial NADH:ubiquinone oxidoreductase 24-kDa gene (NDUFV2) and its pseudogeneR de Coo, P Buddiger, H Smeets, et al.Journal of Medical Genetics|March 10, 2001
Clinical and molecular characterisation of 80 patients with 5p deletion: genotype-phenotype correlationP C Mainardi, C Perfumo, A Calì, et al.Molecular Psychiatry|December 17, 1997
An integrated physical map of 18p11.2: a susceptibility region for bipolar disorderL E Esterling, T Cox Matise, A R Sanders, et al.Human Genetics|April 1, 1996
Ablepharon macrostomia syndrome with associated cutis laxa: possible localization to 18qJ E Pellegrino, R E Schnur, L Boghosian-Sell, et al.Genomics|July 15, 1997
The human gene ZFP161 on 18p11.21-pter encodes a putative c-myc repressor and is homologous to murine Zfp161 (Chr 17) and Zfp161-rs1 (X Chr)I Sobek-Klocke, C Disqué-Kochem, M Ronsiek, et al.Human Molecular Genetics|January 15, 1999
An 18q- syndrome breakpoint resides between the duplicated serpins SCCA1 and SCCA2 and arises via a cryptic rearrangement with satellite III DNAS G Katz, S S Schneider, A Bartuski, et al.Genomics|December 1, 1994
Regional localization of 188 sequence tagged sites on a somatic cell hybrid mapping panel for human chromosome 3R J Leach, R Chinn, B E Reus, et al.Genomics|February 15, 1996
The generation and regional localization of 303 new chromosome 5 sequence-tagged sitesD L Grady, D L Robinson, M Gersh, et al.Genome Research|December 30, 1999
An integrated physical map for the short arm of human chromosome 5E T Peterson, R Sutherland, D L Robinson, et al.Pageof 8