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D W Cox

Showing results (121-130 of 223) with videos related to

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Canadian Medical Association Journal|June 8, 1974
[Alpha-1 antitrypsin deficiency: correlation between biochemical tests and phenotypes in one family]J L Malo, R Daigneault, A Hercz, et al.
Nucleic Acids Research|February 11, 1991
A polymorphism of D13S86 from the region 13q14.1 to 13q22N P McHaffie, R Houwen, W Cavenee, et al.
The EMBO Journal|October 1, 1990
The physical organization of the human immunoglobulin heavy chain gene complexM A Walter, U Surti, M H Hofker, et al.
Human Genetics|October 1, 1990
A multigene deletion in the immunoglobulin heavy chain region in a highly atopic individualM A Walter, C A Chambers, B Zimmerman, et al.
American Journal of Clinical Pathology|October 1, 1984
Occurrence of alpha-1-antitrypsin deficiency in 155 patients with alcoholic liver diseaseE A Roberts, D W Cox, A Medline, et al.
The Biochemical Journal|May 1, 1985
31P-saturation-transfer nuclear-magnetic-resonance measurements of phosphocreatine turnover in guinea-pig brain slicesP G Morris, J Feeney, D W Cox, et al.
Clinical Science and Molecular Medicine|July 1, 1978
Catabolic rate of alpha1-antitrypsin of of Pi types S, and MMalton and of asialylated M-protein in manJ O Jeppsson, C B Laurell, B Nosslin, et al.
The Journal of Pediatrics|January 1, 1976
Liver disease associated with alpha1-antitrypsin deficiency in childhoodS P Moroz, E Cutz, D W Cox, et al.
Clinical Genetics|October 12, 2001
Features within the holoprosencephaly spectrum in sibs with a Robertsonian (14q;22q) translocation chromosomeD Kamnasaran, J A Gerritsen, D R McLeod, et al.
Nature Genetics|August 1, 1994
The LEC rat has a deletion in the copper transporting ATPase gene homologous to the Wilson disease geneJ Wu, J R Forbes, H S Chen, et al.
Pageof 23

Showing results (121-130 of 223) with videos related to

Sort By:
Pageof 23
Canadian Medical Association Journal|June 8, 1974
[Alpha-1 antitrypsin deficiency: correlation between biochemical tests and phenotypes in one family]J L Malo, R Daigneault, A Hercz, et al.
Nucleic Acids Research|February 11, 1991
A polymorphism of D13S86 from the region 13q14.1 to 13q22N P McHaffie, R Houwen, W Cavenee, et al.
The EMBO Journal|October 1, 1990
The physical organization of the human immunoglobulin heavy chain gene complexM A Walter, U Surti, M H Hofker, et al.
Human Genetics|October 1, 1990
A multigene deletion in the immunoglobulin heavy chain region in a highly atopic individualM A Walter, C A Chambers, B Zimmerman, et al.
American Journal of Clinical Pathology|October 1, 1984
Occurrence of alpha-1-antitrypsin deficiency in 155 patients with alcoholic liver diseaseE A Roberts, D W Cox, A Medline, et al.
The Biochemical Journal|May 1, 1985
31P-saturation-transfer nuclear-magnetic-resonance measurements of phosphocreatine turnover in guinea-pig brain slicesP G Morris, J Feeney, D W Cox, et al.
Clinical Science and Molecular Medicine|July 1, 1978
Catabolic rate of alpha1-antitrypsin of of Pi types S, and MMalton and of asialylated M-protein in manJ O Jeppsson, C B Laurell, B Nosslin, et al.
The Journal of Pediatrics|January 1, 1976
Liver disease associated with alpha1-antitrypsin deficiency in childhoodS P Moroz, E Cutz, D W Cox, et al.
Clinical Genetics|October 12, 2001
Features within the holoprosencephaly spectrum in sibs with a Robertsonian (14q;22q) translocation chromosomeD Kamnasaran, J A Gerritsen, D R McLeod, et al.
Nature Genetics|August 1, 1994
The LEC rat has a deletion in the copper transporting ATPase gene homologous to the Wilson disease geneJ Wu, J R Forbes, H S Chen, et al.
Pageof 23