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J C Mulley

Showing results (41-50 of 146) with videos related to

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Brain & Development|November 10, 2001
Clinical and molecular genetics of myoclonic-astatic epilepsy and severe myoclonic epilepsy in infancy (Dravet syndrome)I E Scheffer, R Wallace, J C Mulley, et al.
American Journal of Human Genetics|November 1, 1983
Regional localization for HLA by recombination with a fragile site at 6p23J C Mulley, J Hay, L J Sheffield, et al.
Human Molecular Genetics|November 1, 1994
Ten microsatellite polymorphisms mapped to chromosome 16H A Phillips, S C Gerken, J C Mulley, et al.
American Journal of Medical Genetics|April 1, 1992
Use of linkage data obtained in single families: prenatal diagnosis of a new X-linked mental retardation syndromeJ C Mulley, A K Gedeon, S Wilson, et al.
Human Genetics|February 1, 1988
A regional localisation for an X-linked suppressor gene (XS) for the Lutheran blood groupJ C Mulley, P C Norman, P Tippett, et al.
American Journal of Medical Genetics|April 1, 1992
Characterization of new PCR based markers for mapping and diagnosis: AC dinucleotide repeat markers at the DXS237 (GMGX9) and DXS102 (cX38.1) lociA K Gedeon, K Holman, R I Richards, et al.
Nature Genetics|May 1, 1996
Identification of the gene FMR2, associated with FRAXE mental retardationJ Gecz, A K Gedeon, G R Sutherland, et al.
American Journal of Medical Genetics|July 12, 1996
Genetic localisation of MRX27 to Xq24-26 defines another discrete gene for non-specific X-linked mental retardationA K Gedeon, I A Glass, J M Connor, et al.
Nucleic Acids Research|September 25, 1991
An XmnI RFLP for CYP2A on chromosome 19J A McCure, I R Phillips, E A Shephard, et al.
Australian Paediatric Journal|October 1, 1989
Deletion analysis for Duchenne (and Becker) muscular dystrophyR D Kimber, V J Hyland, E A Haan, et al.
Pageof 15

Showing results (41-50 of 146) with videos related to

Sort By:
Pageof 15
Brain & Development|November 10, 2001
Clinical and molecular genetics of myoclonic-astatic epilepsy and severe myoclonic epilepsy in infancy (Dravet syndrome)I E Scheffer, R Wallace, J C Mulley, et al.
American Journal of Human Genetics|November 1, 1983
Regional localization for HLA by recombination with a fragile site at 6p23J C Mulley, J Hay, L J Sheffield, et al.
Human Molecular Genetics|November 1, 1994
Ten microsatellite polymorphisms mapped to chromosome 16H A Phillips, S C Gerken, J C Mulley, et al.
American Journal of Medical Genetics|April 1, 1992
Use of linkage data obtained in single families: prenatal diagnosis of a new X-linked mental retardation syndromeJ C Mulley, A K Gedeon, S Wilson, et al.
Human Genetics|February 1, 1988
A regional localisation for an X-linked suppressor gene (XS) for the Lutheran blood groupJ C Mulley, P C Norman, P Tippett, et al.
American Journal of Medical Genetics|April 1, 1992
Characterization of new PCR based markers for mapping and diagnosis: AC dinucleotide repeat markers at the DXS237 (GMGX9) and DXS102 (cX38.1) lociA K Gedeon, K Holman, R I Richards, et al.
Nature Genetics|May 1, 1996
Identification of the gene FMR2, associated with FRAXE mental retardationJ Gecz, A K Gedeon, G R Sutherland, et al.
American Journal of Medical Genetics|July 12, 1996
Genetic localisation of MRX27 to Xq24-26 defines another discrete gene for non-specific X-linked mental retardationA K Gedeon, I A Glass, J M Connor, et al.
Nucleic Acids Research|September 25, 1991
An XmnI RFLP for CYP2A on chromosome 19J A McCure, I R Phillips, E A Shephard, et al.
Australian Paediatric Journal|October 1, 1989
Deletion analysis for Duchenne (and Becker) muscular dystrophyR D Kimber, V J Hyland, E A Haan, et al.
Pageof 15