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A P Walker

Showing results (111-120 of 127) with videos related to

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American Journal of Human Genetics|June 1, 1996
Mutations and phenotype in isolated glycerol kinase deficiencyA P Walker, F Muscatelli, A N Stafford, et al.
Clinical Nuclear Medicine|June 1, 1992
Imaging of regional spread of breast cancer by internal mammary lymphoscintigraphy, CT, and MRIH T Turoglu, N A Janjan, M K Thorsen, et al.
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association|March 1, 1995
Comparison of the up-and-down, conventional LD50, and fixed-dose acute toxicity proceduresR L Lipnick, J A Cotruvo, R N Hill, et al.
Human Molecular Genetics|November 1, 1992
A YAC contig in Xp21 containing the adrenal hypoplasia congenita and glycerol kinase deficiency genesA P Walker, J Chelly, D R Love, et al.
Lancet (London, England)|March 4, 1989
Inherited deletion at Duchenne dystrophy locus in normal maleR J Bartlett, A P Walker, N G Laing, et al.
Journal of Medical Genetics|February 1, 1997
Haemochromatosis: a gene at last?K J Robson, J D Shearman, A T Merryweather-Clarke, et al.
Nucleic Acids Research|September 26, 1988
A Bgl II polymorphism detected by LDR152 [D19S19]A P Walker, R J Bartlett, L H Yamaoka, et al.
Human Molecular Genetics|April 1, 1992
Reconstruction of the 2.4 Mb human DMD-gene by homologous YAC recombinationJ T Den Dunnen, P M Grootscholten, J G Dauwerse, et al.
Nucleic Acids Research|November 25, 1991
A StuI polymorphism on chromosome 3p14.1-14.2 (D3S622) defined by two polymorphic StuI sites 2.4 kb apartS L Secore, A P Walker, M H Herbstreith, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|September 29, 2012
Genetic analysis of NR0B1 in congenital adrenal hypoplasia patients: identification of a rare regulatory variant resulting in congenital adrenal hypoplasia and hypogonadal hypogonadism without testicular carcinoma in situA P Walker, R C Fowkes, F Saleh, et al.
Pageof 13

Showing results (111-120 of 127) with videos related to

Sort By:
Pageof 13
American Journal of Human Genetics|June 1, 1996
Mutations and phenotype in isolated glycerol kinase deficiencyA P Walker, F Muscatelli, A N Stafford, et al.
Clinical Nuclear Medicine|June 1, 1992
Imaging of regional spread of breast cancer by internal mammary lymphoscintigraphy, CT, and MRIH T Turoglu, N A Janjan, M K Thorsen, et al.
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association|March 1, 1995
Comparison of the up-and-down, conventional LD50, and fixed-dose acute toxicity proceduresR L Lipnick, J A Cotruvo, R N Hill, et al.
Human Molecular Genetics|November 1, 1992
A YAC contig in Xp21 containing the adrenal hypoplasia congenita and glycerol kinase deficiency genesA P Walker, J Chelly, D R Love, et al.
Lancet (London, England)|March 4, 1989
Inherited deletion at Duchenne dystrophy locus in normal maleR J Bartlett, A P Walker, N G Laing, et al.
Journal of Medical Genetics|February 1, 1997
Haemochromatosis: a gene at last?K J Robson, J D Shearman, A T Merryweather-Clarke, et al.
Nucleic Acids Research|September 26, 1988
A Bgl II polymorphism detected by LDR152 [D19S19]A P Walker, R J Bartlett, L H Yamaoka, et al.
Human Molecular Genetics|April 1, 1992
Reconstruction of the 2.4 Mb human DMD-gene by homologous YAC recombinationJ T Den Dunnen, P M Grootscholten, J G Dauwerse, et al.
Nucleic Acids Research|November 25, 1991
A StuI polymorphism on chromosome 3p14.1-14.2 (D3S622) defined by two polymorphic StuI sites 2.4 kb apartS L Secore, A P Walker, M H Herbstreith, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|September 29, 2012
Genetic analysis of NR0B1 in congenital adrenal hypoplasia patients: identification of a rare regulatory variant resulting in congenital adrenal hypoplasia and hypogonadal hypogonadism without testicular carcinoma in situA P Walker, R C Fowkes, F Saleh, et al.
Pageof 13