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Journal of Medical Genetics|January 1, 1989
21-hydroxylase deficiency families with HLA identical affected and unaffected sibsP J Sinnott, P A Dyer, D A Price, et al.Journal of Medical Genetics|November 1, 1989
Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophyS Hodgson, K Hart, S Abbs, et al.Annals of the Rheumatic Diseases|August 1, 1985
Gm and Km allotypes in rheumatoid arthritisP A Sanders, G G de Lange, P A Dyer, et al.Journal of Medical Genetics|December 1, 1986
Linkage studies in Duchenne and Becker muscular dystrophiesA Walker, K Hart, C Cole, et al.Clinical Genetics|October 1, 1988
PRUFILE: a clinical and laboratory database for the genetics centreD E Mutton, K Chown, L Thomson, et al.American Journal of Medical Genetics|March 1, 1986
A balanced de novo X/autosome translocation in a girl with manifestations of Lowe syndromeS V Hodgson, J Z Heckmatt, E Hughes, et al.Annals of the Rheumatic Diseases|January 1, 1987
Predictive value of mean platelet volume in gold induced thrombocytopeniaP S Klimiuk, P J Holt, R B Clague, et al.Tissue Antigens|August 1, 1982
Absence of linkage between adult polycystic kidney disease and the major histocompatibility systemP A Dyer, E A Watters, P T Klouda, et al.British Heart Journal|January 1, 1994
Do specific HLA antigens predispose to ischaemic heart disease or idiopathic dilated cardiomyopathy?S C Grant, S Sheldon, P A Dyer, et al.Tissue Antigens|September 1, 1995
Definition of HLA-C alleles using sequence-specific oligonucleotide probes (PCR-SSOP)L J Kennedy, K V Poulton, P A Dyer, et al.Pageof 22