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American Journal of Human Genetics|June 23, 1998
A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3G De Michele, M De Fusco, F Cavalcanti, et al.Human Molecular Genetics|June 1, 1992
Characterization of a YAC containing part or all of the Norrie disease locusZ Y Chen, K B Sims, M Coleman, et al.Human Genetics|April 1, 1990
A locus for X-linked congenital stationary night blindness is located on the proximal portion of the short arm of the X chromosomeN T Bech-Hansen, L L Field, A M Schramm, et al.Annals of Human Genetics|January 1, 1989
Molecular characterization of human X/Y translocations suggests their aetiology through aberrant exchange between homologous sequences on Xp and YqA Ballabio, R Carrozzo, A Gil, et al.Proceedings of the National Academy of Sciences of the United States of America|December 1, 1989
Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosomeA Ballabio, B Bardoni, R Carrozzo, et al.Genomics|April 16, 1998
FACL4, a new gene encoding long-chain acyl-CoA synthetase 4, is deleted in a family with Alport syndrome, elliptocytosis, and mental retardationM Piccini, F Vitelli, M Bruttini, et al.Genomics|May 20, 1999
Identification of SCML2, a second human gene homologous to the Drosophila sex comb on midleg (Scm): A new gene cluster on Xp22E Montini, G Buchner, C Spalluto, et al.American Journal of Human Genetics|October 1, 1990
Definitive localization of X-linked Kallman syndrome (hypogonadotropic hypogonadism and anosmia) to Xp22.3: close linkage to the hypervariable repeat sequence CRI-S232T Meitinger, B Heye, C Petit, et al.The Biochemical Journal|June 22, 2000
Identification and expression of NEU3, a novel human sialidase associated to the plasma membraneE Monti, M T Bassi, N Papini, 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.Pageof 30