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J C Mulley

Showing results (71-80 of 146) with videos related to

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Human Molecular Genetics|November 1, 1992
Identification of a highly polymorphic marker within intron 7 of the ALAS2 gene and suggestion of at least two loci for X-linked sideroblastic anemiaT C Cox, H M Kozman, W H Raskind, et al.
Journal of Medical Genetics|July 1, 1991
Predictive diagnosis of myotonic dystrophy with flanking microsatellite markersJ C Mulley, A K Gedeon, S J White, et al.
Journal of Medical Genetics|April 1, 1989
Becker muscular dystrophy (BMD) and Klinefelter's syndrome: a possible cause of variable expression of BMD within a pedigreeG K Suthers, J I Manson, L M Stern, et al.
Cytogenetics and Cell Genetics|January 1, 1993
A microsatellite marker within the duplicated D16S79 locus has a null allele; significance for linkage mappingH A Phillips, A D Thompson, H M Kozman, et al.
Journal of Medical Genetics|April 1, 1996
Suggestion of a major gene for familial febrile convulsions mapping to 8q13-21R H Wallace, S F Berkovic, R A Howell, et al.
The Medical Journal of Australia|September 19, 1988
Presymptomatic testing for myotonic dystrophy by means of the linked DNA marker APOC2E A Haan, J C Mulley, A K Gedeon, et al.
Genomics|October 14, 2000
Gene structure and expression study of the SEDL gene for spondyloepiphyseal dysplasia tardaJ Gécz, M A Hillman, A K Gedeon, et al.
Journal of Medical Genetics|August 1, 1987
Molecular genetics of human chromosome 16G R Sutherland, S Reeders, V J Hyland, et al.
Australian and New Zealand Journal of Medicine|December 1, 1987
Demonstration of a recent mutation in a family with isolated hemophilia AZ Rudzki, S E Rodgers, G Casey, et al.
American Journal of Human Genetics|November 1, 1993
Genotype-phenotype relationships in fragile X syndrome: a family studyD Z Loesch, R Huggins, D A Hay, et al.
Pageof 15

Showing results (71-80 of 146) with videos related to

Sort By:
Pageof 15
Human Molecular Genetics|November 1, 1992
Identification of a highly polymorphic marker within intron 7 of the ALAS2 gene and suggestion of at least two loci for X-linked sideroblastic anemiaT C Cox, H M Kozman, W H Raskind, et al.
Journal of Medical Genetics|July 1, 1991
Predictive diagnosis of myotonic dystrophy with flanking microsatellite markersJ C Mulley, A K Gedeon, S J White, et al.
Journal of Medical Genetics|April 1, 1989
Becker muscular dystrophy (BMD) and Klinefelter's syndrome: a possible cause of variable expression of BMD within a pedigreeG K Suthers, J I Manson, L M Stern, et al.
Cytogenetics and Cell Genetics|January 1, 1993
A microsatellite marker within the duplicated D16S79 locus has a null allele; significance for linkage mappingH A Phillips, A D Thompson, H M Kozman, et al.
Journal of Medical Genetics|April 1, 1996
Suggestion of a major gene for familial febrile convulsions mapping to 8q13-21R H Wallace, S F Berkovic, R A Howell, et al.
The Medical Journal of Australia|September 19, 1988
Presymptomatic testing for myotonic dystrophy by means of the linked DNA marker APOC2E A Haan, J C Mulley, A K Gedeon, et al.
Genomics|October 14, 2000
Gene structure and expression study of the SEDL gene for spondyloepiphyseal dysplasia tardaJ Gécz, M A Hillman, A K Gedeon, et al.
Journal of Medical Genetics|August 1, 1987
Molecular genetics of human chromosome 16G R Sutherland, S Reeders, V J Hyland, et al.
Australian and New Zealand Journal of Medicine|December 1, 1987
Demonstration of a recent mutation in a family with isolated hemophilia AZ Rudzki, S E Rodgers, G Casey, et al.
American Journal of Human Genetics|November 1, 1993
Genotype-phenotype relationships in fragile X syndrome: a family studyD Z Loesch, R Huggins, D A Hay, et al.
Pageof 15