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Journal of Medical Genetics|October 1, 1988
A deletion of one nucleotide results in functional deficiency of apolipoprotein CII (apo CII Toronto)D W Cox, D E Wills, F Quan, et al.The Biochemical Journal|May 15, 1983
31P-n.m.r. studies on cerebral energy metabolism under conditions of hypoglycaemia and hypoxia in vitroD W Cox, P G Morris, J Feeney, et al.Atherosclerosis|August 1, 1982
Apolipoprotein and lipoprotein concentrations in familial apolipoprotein C-II deficiencyW C Breckenridge, P Alaupovic, D W Cox, et al.Immunogenetics|January 1, 1992
Involvement of both HLA and Ig heavy chain haplotypes in human IgA deficiencyP G Olsson, L Hammarström, D W Cox, et al.Human Genetics|November 1, 1989
Deletion/frameshift mutation in the alpha 1-antitrypsin null allele, PI*QOboltonG C Fraizer, M Siewertsen, T R Harrold, et al.Current Problems in Cancer|February 21, 2018
The challenge of treating older patients with pancreaticobiliary malignanciesLynda R Corrigan, Dara M Bracken-Clarke, Anne M HorganThe Journal of Mental Health Policy and Economics|September 30, 2025
Changes in Access to Substance Use Disorder Treatment Associated with the 2008 U.S. Parity LawTimothy B Creedon, Constance M Horgan, Xiaodong Liu, et al.American Journal of Human Genetics|February 1, 1993
Physical mapping of four serpin genes: alpha 1-antitrypsin, alpha 1-antichymotrypsin, corticosteroid-binding globulin, and protein C inhibitor, within a 280-kb region on chromosome I4q32.1G D Billingsley, M A Walter, G L Hammond, et al.Human Molecular Genetics|October 1, 1994
A heat shock gene at 14q22: mapping and expressionA F Roux, V T Nguyen, J A Squire, et al.Journal of Hepatology|March 1, 1993
DNA markers for the diagnosis of Wilson diseaseR H Houwen, E A Roberts, G R Thomas, et al.Pageof 37