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Nucleic Acids Research
|
September 25, 1991
Dinucleotide repeat polymorphisms at the DXS294 and DXS300 loci in Xq26
A K Gedeon, R I Richards, J C Mulley
Genes, Brain, and Behavior
|
June 15, 2007
A polygenic heterogeneity model for common epilepsies with complex genetics
L M Dibbens, S E Heron, J C Mulley
Annales De Genetique
|
January 1, 1980
Additions to the exclusion map of man
J 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 handicap
G R Sutherland, J C Mulley, R I Richards
American Journal of Medical Genetics
|
April 1, 1992
Nomenclature guidelines for X-linked mental retardation
J C Mulley, B Kerr, R Stevenson, et al.
Biochemical Genetics
|
February 1, 1979
Allozyme genotype--environment relationships in natural populations of Drosophila buzzatii
J C Mulley, J W James, J S Barker
Human Genetics
|
January 1, 1983
A new allele of alpha 1-antitrypsin: PI NADELAIDE
J C Mulley, D W Cox, G R Sutherland
Nucleic Acids Research
|
June 26, 1989
XmnI, HincII and BclI RFLPs at D16S79
A K Gedeon, J C Mulley, M H Breuning
Genetics
|
January 1, 1995
Reduced genetic load revealed by slow inbreeding in Drosophila melanogaster
B 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 activators
J Gecz, S Bielby, G R Sutherland, et al.
Page
of 15
Search research articles
Search
Showing results (31-40 of 146) with videos related to
Sort By:
Page
of 15
Nucleic Acids Research
|
September 25, 1991
Dinucleotide repeat polymorphisms at the DXS294 and DXS300 loci in Xq26
A K Gedeon, R I Richards, J C Mulley
Genes, Brain, and Behavior
|
June 15, 2007
A polygenic heterogeneity model for common epilepsies with complex genetics
L M Dibbens, S E Heron, J C Mulley
Annales De Genetique
|
January 1, 1980
Additions to the exclusion map of man
J 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 handicap
G R Sutherland, J C Mulley, R I Richards
American Journal of Medical Genetics
|
April 1, 1992
Nomenclature guidelines for X-linked mental retardation
J C Mulley, B Kerr, R Stevenson, et al.
Biochemical Genetics
|
February 1, 1979
Allozyme genotype--environment relationships in natural populations of Drosophila buzzatii
J C Mulley, J W James, J S Barker
Human Genetics
|
January 1, 1983
A new allele of alpha 1-antitrypsin: PI NADELAIDE
J C Mulley, D W Cox, G R Sutherland
Nucleic Acids Research
|
June 26, 1989
XmnI, HincII and BclI RFLPs at D16S79
A K Gedeon, J C Mulley, M H Breuning
Genetics
|
January 1, 1995
Reduced genetic load revealed by slow inbreeding in Drosophila melanogaster
B 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 activators
J Gecz, S Bielby, G R Sutherland, et al.
Page
of 15