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J C Mulley

Showing results (51-60 of 146) with videos related to

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Human Genetics|November 1, 1987
Determining the origin of human X isochromosomes by use of DNA sequence polymorphisms and detection of an apparent i(Xq) with Xp sequencesD F Callen, J C Mulley, E G Baker, et al.
The Medical Journal of Australia|March 19, 1990
Predictive diagnosis for polycystic kidney disease using DNA markersJ C Mulley, E A Haan, A K Gedeon, et al.
American Journal of Medical Genetics|July 12, 1996
Regional localisation of two non-specific X-linked mental retardation genes (MRX30 and MRX31)A J Donnelly, M W Partington, A K Ryan, et al.
Human Genetics|March 1, 1988
Recombination frequencies between Duchenne muscular dystrophy and intragenic markers in multigeneration familiesJ C Mulley, E A Haan, L J Sheffield, et al.
Annals of Neurology|June 14, 2000
Locus for febrile seizuresI E Scheffer, R H Wallace, J C Mulley, et al.
American Journal of Medical Genetics|March 2, 1999
Gene localization for oral-facial-digital syndrome type 1 (OFD1:MIM 311200) proximal to DXS85A K Gedeon, C Oley, J Nelson, et al.
Clinical Genetics|July 1, 1985
Genetic linkage analysis of epidermolysis bullosa dystrophica, Cockayne-Touraine typeJ C Mulley, T Turner, C Nicholls, et al.
American Journal of Medical Genetics|August 1, 1994
Localisation of the gene for X-linked reticulate pigmentary disorder with systemic manifestations (PDR), previously known as X-linked cutaneous amyloidosisA K Gedeon, J C Mulley, H Kozman, et al.
American Journal of Medical Genetics|July 12, 1996
How many X-linked genes for non-specific mental retardation (MRX) are there?A K Gedeon, A J Donnelly, J C Mulley, et al.
American Journal of Medical Genetics|May 1, 1988
A family with the Coffin Lowry syndrome revisited: localization of CLS to Xp21-pterM W Partington, J C Mulley, G R Sutherland, et al.
Pageof 15

Showing results (51-60 of 146) with videos related to

Sort By:
Pageof 15
Human Genetics|November 1, 1987
Determining the origin of human X isochromosomes by use of DNA sequence polymorphisms and detection of an apparent i(Xq) with Xp sequencesD F Callen, J C Mulley, E G Baker, et al.
The Medical Journal of Australia|March 19, 1990
Predictive diagnosis for polycystic kidney disease using DNA markersJ C Mulley, E A Haan, A K Gedeon, et al.
American Journal of Medical Genetics|July 12, 1996
Regional localisation of two non-specific X-linked mental retardation genes (MRX30 and MRX31)A J Donnelly, M W Partington, A K Ryan, et al.
Human Genetics|March 1, 1988
Recombination frequencies between Duchenne muscular dystrophy and intragenic markers in multigeneration familiesJ C Mulley, E A Haan, L J Sheffield, et al.
Annals of Neurology|June 14, 2000
Locus for febrile seizuresI E Scheffer, R H Wallace, J C Mulley, et al.
American Journal of Medical Genetics|March 2, 1999
Gene localization for oral-facial-digital syndrome type 1 (OFD1:MIM 311200) proximal to DXS85A K Gedeon, C Oley, J Nelson, et al.
Clinical Genetics|July 1, 1985
Genetic linkage analysis of epidermolysis bullosa dystrophica, Cockayne-Touraine typeJ C Mulley, T Turner, C Nicholls, et al.
American Journal of Medical Genetics|August 1, 1994
Localisation of the gene for X-linked reticulate pigmentary disorder with systemic manifestations (PDR), previously known as X-linked cutaneous amyloidosisA K Gedeon, J C Mulley, H Kozman, et al.
American Journal of Medical Genetics|July 12, 1996
How many X-linked genes for non-specific mental retardation (MRX) are there?A K Gedeon, A J Donnelly, J C Mulley, et al.
American Journal of Medical Genetics|May 1, 1988
A family with the Coffin Lowry syndrome revisited: localization of CLS to Xp21-pterM W Partington, J C Mulley, G R Sutherland, et al.
Pageof 15