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FEBS Letters|September 15, 1986
Aggregation of plasma Z type alpha 1-antitrypsin suggests basic defect for the deficiencyD W Cox, G D Billingsley, J W CallahanAmerican Journal of Human Genetics|November 1, 1985
A multigene deletion within the immunoglobulin heavy-chain regionH Chaabani, N T Bech-Hansen, D W CoxGerontology|January 1, 1987
Nuclear magnetic resonance as a tool to study brain metabolismH S Bachelard, D W Cox, P G MorrisThe New England Journal of Medicine|December 28, 1978
Inheritance of apolipoprotein C-II deficiency with hypertriglyceridemia and pancreatitisD W Cox, W C Breckenridge, J A LittleThe Journal of Experimental Medicine|August 1, 1991
A deletion map of the human immunoglobulin heavy chain variable regionM A Walter, H M Dosch, D W CoxAmerican Journal of Human Genetics|July 1, 1994
Physical and genetic mapping of the serpin gene cluster at 14q32.1: allelic association and a unique haplotype associated with alpha 1-antitrypsin deficiencyB C Byth, G D Billingsley, D W CoxImmunogenetics|January 1, 1995
Defining the breakpoint of a multigene deletion in the immunoglobulin heavy chain gene clusterZ Q Chen, M H Hofker, D W CoxProceedings of the National Academy of Sciences of the United States of America|July 1, 1989
Complete physical map of the human immunoglobulin heavy chain constant region gene complexM H Hofker, M A Walter, D W CoxAmerican Journal of Human Genetics|May 1, 1986
Genetic polymorphism of alpha 2HS-glycoproteinD W Cox, B J Andrews, D E WillsCytogenetics and Cell Genetics|April 25, 2000
Cloning and mapping of murine superoxide dismutase copper chaperone (Ccsd) and mapping of the human orthologS D Moore, M M Chen, D W CoxPageof 30