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Nature|January 21, 1993
The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinasesD Vetrie, I Vorechovský, P Sideras, et al.Human Genetics|March 1, 1987
Prenatal diagnosis of X-linked choroideremia with mental retardation, associated with a cytologically detectable X-chromosome deletionS V Hodgson, M E Robertson, C N Fear, et al.European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics|August 12, 2000
Mannose binding lectin (MBL) genotype distributions with relation to serum levels in UK CaucasoidsD J Crosdale, W E Ollier, W Thomson, et al.Nature Genetics|June 1, 1996
Characterization of DRP2, a novel human dystrophin homologueR G Roberts, T C Freeman, E Kendall, et al.American Journal of Obstetrics and Gynecology|November 1, 1983
Gonadotropins and gonadal steroids in androgen insensitivity (testicular feminization) syndrome: effects of castration and sex steroid administrationF Naftolin, P Pujol-Amat, C S Corker, et al.Genomics|January 1, 1994
A 6.5-Mb yeast artificial chromosome contig incorporating 33 DNA markers on the human X chromosome at Xq22D Vetrie, E Kendall, A Coffey, et al.Annals of the Rheumatic Diseases|May 1, 1987
Gm allotypes and HLA in rheumatoid arthritis patients with circulating antibodies to native type II collagenP A Sanders, D M Grennan, P S Klimiuk, et al.Arthritis and Rheumatism|May 1, 1994
"Homozygosity" for the HLA-DR shared epitope contributes the highest risk for rheumatoid arthritis concordance in identical twinsD Jawaheer, W Thomson, A J MacGregor, et al.Annals of the Rheumatic Diseases|April 1, 1995
Lack of influence of non-inherited maternal HLA-DR alleles on susceptibility to rheumatoid arthritisA J Silman, E M Hay, J Worthington, et al.Journal of Medical Genetics|November 1, 1994
Deletions in the 5' region of dystrophin and resulting phenotypesF Muntoni, P Gobbi, C Sewry, et al.Pageof 22