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Clinical Genetics|February 1, 1980
Association of severe rheumatoid arthritis with heterozygosity for alpha 1-antitrypsin deficiencyD W Cox, O HuberJournal of Medical Genetics|January 1, 1987
Prenatal diagnosis of alpha 1 antitrypsin deficiency and estimates of fetal risk for diseaseD W Cox, T MansfieldThe American Review of Respiratory Disease|February 1, 1988
Emphysema of early onset associated with a complete deficiency of alpha-1-antitrypsin (null homozygotes)D W Cox, H LevisonHuman Heredity|January 1, 1988
Genetic characterization and origin of Tunisian BerbersH Chaâbani, D W CoxPreparative Biochemistry|January 1, 1980
Purification of rat ceruloplasmin. characterization and comparison with human ceruloplasminA Manolis, D W CoxMethods in Molecular Biology (Clifton, N.J.)|March 17, 2011
Two-Dimensional DNA Electrophoresis (2D-DE) for Mammalian DNAM A Walter, D W CoxGenomics|December 10, 1999
The copper chaperone Atox1 in canine copper toxicosis in Bedlington terriersM S Nanji, D W CoxBrain Research|May 13, 1982
Attenuation of evoked field potentials from dentate granule cells by low glucose, pyruvate + malate, and sodium fluorideD W Cox, H S BachelardBrain Research|February 2, 1988
On the relationship between the excitability of dentate granule cell field potentials and their sensitivity to low glucoseD W Cox, H S BachelardPageof 37