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Cytogenetics and Cell Genetics|January 1, 1996
Chromosomal evolution in duiker antelope (Cephalophinae: Bovidae): karyotype comparisons, fluorescence in situ hybridization, and rampant X chromosome variationT J Robinson, V Wilson, D S Gallagher, et al.Genomics|March 1, 1997
Human glutamate pyruvate transaminase (GPT): localization to 8q24.3, cDNA and genomic sequences, and polymorphic sitesM M Sohocki, L S Sullivan, W R Harrison, et al.American Journal of Human Genetics|December 1, 1991
Molecular confirmation of Wolf-Hirschhorn syndrome with a subtle translocation of chromosome 4M R Altherr, U Bengtsson, F F Elder, et al.Genomics|December 15, 1996
Characterization of human DSPG3, a small dermatan sulfate proteoglycanM Deere, J Johnson, S Garza, et al.Genomics|September 1, 1995
A 4-megabase YAC contig that spans the Langer-Giedion syndrome region on human chromosome 8q24.1: use in refining the location of the trichorhinophalangeal syndrome and multiple exostoses genes (TRPS1 and EXT1)J Hou, J Parrish, H J Lüdecke, et al.American Journal of Human Genetics|October 27, 1997
Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndromeS K Shapira, C McCaskill, H Northrup, et al.Genomics|October 27, 1999
Insertional mutation of the collagen genes Col4a3 and Col4a4 in a mouse model of Alport syndromeW Lu, C L Phillips, P D Killen, et al.Nature Genetics|July 1, 1995
Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasiaJ T Hecht, L D Nelson, E Crowder, et al.Prenatal Diagnosis|April 1, 1996
Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicismS L Christian, A C Smith, M Macha, et al.Nature Genetics|October 15, 1998
Inversin, a novel gene in the vertebrate left-right axis pathway, is partially deleted in the inv mouseD Morgan, L Turnpenny, J Goodship, et al.Pageof 6