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J Mulley

Showing results (1-10 of 28) with videos related to

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Genome Research|February 15, 2000
Genes for cognitive function: developments on the XJ Gécz, J Mulley
American Journal of Medical Genetics|July 12, 1996
Gene localisation for Sutherland-Haan syndrome (SHS:MIM 309470)A Gedeon, J Mulley, E Haan
American Journal of Medical Genetics|July 12, 1996
Gene localisation for Wilson-Turner syndrome (WTS:MIM 309585)A Gedeon, J Mulley, G Turner
American Journal of Medical Genetics|July 15, 1994
X-linked mental retardation with dystonic movements of the hands (PRTS): revisitedA Gedeon, M Partington, J Mulley
Journal of the National Cancer Institute|March 12, 2009
Why are a high overdiagnosis probability and a long lead time for prostate cancer screening so important?Michael J Barry, Albert J Mulley
American Journal of Medical Genetics|July 15, 1994
X-linked mental retardation with heterozygous expression and macrocephaly: pericentromeric gene localizationG Turner, A Gedeon, J Mulley
Human Mutation|April 24, 1999
A novel mutation in exon b (R259C) of the MTM1 gene is associated with a mild myotubular myopathy. Mutation in brief no. 125. OnlineA Donnelly, E Haan, J Manson, et al.
American Journal of Medical Genetics|July 15, 1994
Pericentromeric genes for non-specific X-linked mental retardation (MRX)A Gedeon, B Kerr, J Mulley, et al.
American Journal of Medical Genetics|July 15, 1994
Transmitting males and carrier females in fragile X--revisitedD Z Loesch, D A Hay, J Mulley
Human Mutation|January 1, 1996
A novel mutation in exon 6 (F236S) of the proteolipid protein gene is associated with spastic paraplegiaA Donnelly, A Colley, D Crimmins, et al.
Pageof 3

Showing results (1-10 of 28) with videos related to

Sort By:
Pageof 3
Genome Research|February 15, 2000
Genes for cognitive function: developments on the XJ Gécz, J Mulley
American Journal of Medical Genetics|July 12, 1996
Gene localisation for Sutherland-Haan syndrome (SHS:MIM 309470)A Gedeon, J Mulley, E Haan
American Journal of Medical Genetics|July 12, 1996
Gene localisation for Wilson-Turner syndrome (WTS:MIM 309585)A Gedeon, J Mulley, G Turner
American Journal of Medical Genetics|July 15, 1994
X-linked mental retardation with dystonic movements of the hands (PRTS): revisitedA Gedeon, M Partington, J Mulley
Journal of the National Cancer Institute|March 12, 2009
Why are a high overdiagnosis probability and a long lead time for prostate cancer screening so important?Michael J Barry, Albert J Mulley
American Journal of Medical Genetics|July 15, 1994
X-linked mental retardation with heterozygous expression and macrocephaly: pericentromeric gene localizationG Turner, A Gedeon, J Mulley
Human Mutation|April 24, 1999
A novel mutation in exon b (R259C) of the MTM1 gene is associated with a mild myotubular myopathy. Mutation in brief no. 125. OnlineA Donnelly, E Haan, J Manson, et al.
American Journal of Medical Genetics|July 15, 1994
Pericentromeric genes for non-specific X-linked mental retardation (MRX)A Gedeon, B Kerr, J Mulley, et al.
American Journal of Medical Genetics|July 15, 1994
Transmitting males and carrier females in fragile X--revisitedD Z Loesch, D A Hay, J Mulley
Human Mutation|January 1, 1996
A novel mutation in exon 6 (F236S) of the proteolipid protein gene is associated with spastic paraplegiaA Donnelly, A Colley, D Crimmins, et al.
Pageof 3