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J C Mulley

Showing results (31-40 of 146) with videos related to

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Nucleic Acids Research|September 25, 1991
Dinucleotide repeat polymorphisms at the DXS294 and DXS300 loci in Xq26A K Gedeon, R I Richards, J C Mulley
Genes, Brain, and Behavior|June 15, 2007
A polygenic heterogeneity model for common epilepsies with complex geneticsL M Dibbens, S E Heron, J C Mulley
Annales De Genetique|January 1, 1980
Additions to the exclusion map of manJ C Mulley, G D Bryant, G R Sutherland
The Medical Journal of Australia|April 5, 1993
Fragile X syndrome. The most common cause of familial intellectual handicapG R Sutherland, J C Mulley, R I Richards
American Journal of Medical Genetics|April 1, 1992
Nomenclature guidelines for X-linked mental retardationJ C Mulley, B Kerr, R Stevenson, et al.
Biochemical Genetics|February 1, 1979
Allozyme genotype--environment relationships in natural populations of Drosophila buzzatiiJ C Mulley, J W James, J S Barker
Human Genetics|January 1, 1983
A new allele of alpha 1-antitrypsin: PI NADELAIDEJ C Mulley, D W Cox, G R Sutherland
Nucleic Acids Research|June 26, 1989
XmnI, HincII and BclI RFLPs at D16S79A K Gedeon, J C Mulley, M H Breuning
Genetics|January 1, 1995
Reduced genetic load revealed by slow inbreeding in Drosophila melanogasterB D Latter, J C Mulley, D Reid, et al.
Genomics|September 23, 1997
Gene structure and subcellular localization of FMR2, a member of a new family of putative transcription activatorsJ Gecz, S Bielby, G R Sutherland, et al.
Pageof 15

Showing results (31-40 of 146) with videos related to

Sort By:
Pageof 15
Nucleic Acids Research|September 25, 1991
Dinucleotide repeat polymorphisms at the DXS294 and DXS300 loci in Xq26A K Gedeon, R I Richards, J C Mulley
Genes, Brain, and Behavior|June 15, 2007
A polygenic heterogeneity model for common epilepsies with complex geneticsL M Dibbens, S E Heron, J C Mulley
Annales De Genetique|January 1, 1980
Additions to the exclusion map of manJ C Mulley, G D Bryant, G R Sutherland
The Medical Journal of Australia|April 5, 1993
Fragile X syndrome. The most common cause of familial intellectual handicapG R Sutherland, J C Mulley, R I Richards
American Journal of Medical Genetics|April 1, 1992
Nomenclature guidelines for X-linked mental retardationJ C Mulley, B Kerr, R Stevenson, et al.
Biochemical Genetics|February 1, 1979
Allozyme genotype--environment relationships in natural populations of Drosophila buzzatiiJ C Mulley, J W James, J S Barker
Human Genetics|January 1, 1983
A new allele of alpha 1-antitrypsin: PI NADELAIDEJ C Mulley, D W Cox, G R Sutherland
Nucleic Acids Research|June 26, 1989
XmnI, HincII and BclI RFLPs at D16S79A K Gedeon, J C Mulley, M H Breuning
Genetics|January 1, 1995
Reduced genetic load revealed by slow inbreeding in Drosophila melanogasterB D Latter, J C Mulley, D Reid, et al.
Genomics|September 23, 1997
Gene structure and subcellular localization of FMR2, a member of a new family of putative transcription activatorsJ Gecz, S Bielby, G R Sutherland, et al.
Pageof 15