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D F Callen

Showing results (161-170 of 195) with videos related to

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Journal of Medical Genetics|October 1, 1990
Map of 16 polymorphic loci on the short arm of chromosome 16 close to the polycystic kidney disease gene (PKD1)M H Breuning, F G Snijdewint, H Brunner, et al.
The Journal of Biological Chemistry|October 4, 1996
Molecular cloning of the cDNA and chromosome localization of the gene for human ubiquitin-conjugating enzyme 9Z Y Wang, Q Q Qiu, W Seufert, et al.
Human Genetics|February 1, 1990
Probe, VK5B, is located in the same interval as the autosomal dominant adult polycystic kidney disease locus, PKD1V J Hyland, G K Suthers, K Friend, et al.
Annals of Human Genetics|January 1, 1990
Isolation and use of chromosome 1 probes for linkage studies on Charcot-Marie-Tooth diseaseL R Griffiths, M B Zwi, N Mesterovic, et al.
American Journal of Human Genetics|August 1, 1990
Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell linesG K Suthers, V J Hyland, D F Callen, et al.
Biochemical and Biophysical Research Communications|November 30, 1994
Mapping of two phenol sulphotransferase genes, STP and STM, to 16p: candidate genes for Batten diseaseT P Dooley, H M Mitchison, P B Munroe, et al.
Human Genetics|August 1, 1988
Interleukin 4 is at 5q31 and interleukin 6 is at 7p15G R Sutherland, E Baker, D F Callen, et al.
Biochemistry|May 3, 1988
Structure and chromosomal localization of the human renal kallikrein geneB A Evans, Z X Yun, J A Close, et al.
Human Genetics|March 1, 1991
Frequent deletions at Xq28 indicate genetic heterogeneity in Hunter syndromeP J Wilson, G K Suthers, D F Callen, et al.
Nature Genetics|April 16, 1998
A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosisM Town, G Jean, S Cherqui, et al.
Pageof 20

Showing results (161-170 of 195) with videos related to

Sort By:
Pageof 20
Journal of Medical Genetics|October 1, 1990
Map of 16 polymorphic loci on the short arm of chromosome 16 close to the polycystic kidney disease gene (PKD1)M H Breuning, F G Snijdewint, H Brunner, et al.
The Journal of Biological Chemistry|October 4, 1996
Molecular cloning of the cDNA and chromosome localization of the gene for human ubiquitin-conjugating enzyme 9Z Y Wang, Q Q Qiu, W Seufert, et al.
Human Genetics|February 1, 1990
Probe, VK5B, is located in the same interval as the autosomal dominant adult polycystic kidney disease locus, PKD1V J Hyland, G K Suthers, K Friend, et al.
Annals of Human Genetics|January 1, 1990
Isolation and use of chromosome 1 probes for linkage studies on Charcot-Marie-Tooth diseaseL R Griffiths, M B Zwi, N Mesterovic, et al.
American Journal of Human Genetics|August 1, 1990
Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell linesG K Suthers, V J Hyland, D F Callen, et al.
Biochemical and Biophysical Research Communications|November 30, 1994
Mapping of two phenol sulphotransferase genes, STP and STM, to 16p: candidate genes for Batten diseaseT P Dooley, H M Mitchison, P B Munroe, et al.
Human Genetics|August 1, 1988
Interleukin 4 is at 5q31 and interleukin 6 is at 7p15G R Sutherland, E Baker, D F Callen, et al.
Biochemistry|May 3, 1988
Structure and chromosomal localization of the human renal kallikrein geneB A Evans, Z X Yun, J A Close, et al.
Human Genetics|March 1, 1991
Frequent deletions at Xq28 indicate genetic heterogeneity in Hunter syndromeP J Wilson, G K Suthers, D F Callen, et al.
Nature Genetics|April 16, 1998
A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosisM Town, G Jean, S Cherqui, et al.
Pageof 20