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The American Review of Respiratory Disease|January 1, 1980
Functional assay of alpha 1-antitrypsin in obstructive lung diseaseG D Billingsley, D W CoxHuman Genetics|January 1, 1982
Functional assessment of genetic variants of alpha 1-antitrypsinG D Billingsley, D W CoxThe American Review of Respiratory Disease|October 1, 1984
Oxidation of plasma alpha 1-antitrypsin in smokers and nonsmokers and by an oxidizing agentD W Cox, G D BillingsleyAmerican Journal of Human Genetics|June 1, 1989
Rare deficiency types of alpha 1-antitrypsin: electrophoretic variation and DNA haplotypesD W Cox, G D BillingsleyAmerican Journal of Human Genetics|November 1, 1987
DNA restriction-site polymorphisms associated with the alpha 1-antitrypsin geneD W Cox, G D Billingsley, T MansfieldAmerican 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 CoxFEBS 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|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.Cytogenetics and Cell Genetics|January 1, 1994
Regional localization of loci on chromosome 14 using somatic cell hybridsG D Billingsley, D W Cox, A M Duncan, et al.American Journal of Human Genetics|October 16, 1999
The gamma-crystallins and human cataracts: a puzzle made clearerE Héon, M Priston, D F Schorderet, et al.Pageof 2