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D W Cox

Showing results (131-140 of 223) with videos related to

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Human Mutation|January 1, 1997
24 bp deletion and Ala1278 to Val mutation of the ATP7B gene in a Sardinian family with Wilson diseaseS Orrù, G Thomas, A Loizedda, et al.
Journal of Medical Genetics|April 1, 1985
An autosomal dominant syndrome with 'acromegaloid' features and thickened oral mucosaH E Hughes, P J McAlpine, D W Cox, et al.
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.
Cytogenetics and Cell Genetics|January 1, 1985
Cystic fibrosis: analysis of linkage of the disease locus to red cell and plasma protein markersL C Tsui, D W Cox, P J McAlpine, et al.
Nucleic Acids Research|February 25, 1991
Identification of a polymorphism in human CD44H K Dadi, A M Greaves, D W Cox, et al.
Nucleic Acids Research|May 11, 1994
Application of inverse PCR to isolation of end probes from cosmidsB C Byth, G R Thomas, N Hofland, 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.
Pageof 23

Showing results (131-140 of 223) with videos related to

Sort By:
Pageof 23
Human Mutation|January 1, 1997
24 bp deletion and Ala1278 to Val mutation of the ATP7B gene in a Sardinian family with Wilson diseaseS Orrù, G Thomas, A Loizedda, et al.
Journal of Medical Genetics|April 1, 1985
An autosomal dominant syndrome with 'acromegaloid' features and thickened oral mucosaH E Hughes, P J McAlpine, D W Cox, et al.
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.
Cytogenetics and Cell Genetics|January 1, 1985
Cystic fibrosis: analysis of linkage of the disease locus to red cell and plasma protein markersL C Tsui, D W Cox, P J McAlpine, et al.
Nucleic Acids Research|February 25, 1991
Identification of a polymorphism in human CD44H K Dadi, A M Greaves, D W Cox, et al.
Nucleic Acids Research|May 11, 1994
Application of inverse PCR to isolation of end probes from cosmidsB C Byth, G R Thomas, N Hofland, 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.
Pageof 23