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I W Craig

Showing results (101-110 of 132) with videos related to

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American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 1, 2008
No association with the 5,10-methylenetetrahydrofolate reductase gene and major depressive disorder: results of the depression case control (DeCC) study and a meta-analysisD Gaysina, S Cohen, N Craddock, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 25, 2005
Association analysis of monoamine genes with measures of depression and anxiety in a selected community sample of siblingsM W Nash, K Sugden, P Huezo-Diaz, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 20, 1982
Platelet monoamine oxidase: specific activity and turnover number in headacheK M Summers, G K Brown, I W Craig, et al.
Human Mutation|January 1, 1997
Two new mutations in exon 3 of the NDP gene: S73X and S101F associated with severe and less severe ocular phenotype, respectivelyJ L Walker, J Dixon, C R Fenton, et al.
Nature Genetics|June 1, 1992
Isolation and characterization of a candidate gene for Norrie diseaseZ Y Chen, R W Hendriks, M A Jobling, et al.
Human Molecular Genetics|June 1, 1992
Characterization of a YAC containing part or all of the Norrie disease locusZ Y Chen, K B Sims, M Coleman, et al.
Human Genetics|April 1, 1990
A locus for X-linked congenital stationary night blindness is located on the proximal portion of the short arm of the X chromosomeN T Bech-Hansen, L L Field, A M Schramm, et al.
Human Genetics|December 1, 1991
Analysis of X-chromosome inactivation and presumptive expression of the Wiskott-Aldrich syndrome (WAS) gene in hematopoietic cell lineages of a thrombocytopenic carrier female of WASL D Notarangelo, O Parolini, F Porta, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Mapping the X chromosome breakpoint in two papillary renal cell carcinoma cell lines with a t(X;1)(p11.2;q21.2) and the first report of a female caseJ M Shipley, S Birdsall, J Clark, et al.
Human Genetics|May 1, 1992
Wiskott-Aldrich syndrome carrier detection with the hypervariable marker M27 betaG de Saint Basile, L D Notarangelo, C Bonaiti-Pellié, et al.
Pageof 14

Showing results (101-110 of 132) with videos related to

Sort By:
Pageof 14
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 1, 2008
No association with the 5,10-methylenetetrahydrofolate reductase gene and major depressive disorder: results of the depression case control (DeCC) study and a meta-analysisD Gaysina, S Cohen, N Craddock, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 25, 2005
Association analysis of monoamine genes with measures of depression and anxiety in a selected community sample of siblingsM W Nash, K Sugden, P Huezo-Diaz, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 20, 1982
Platelet monoamine oxidase: specific activity and turnover number in headacheK M Summers, G K Brown, I W Craig, et al.
Human Mutation|January 1, 1997
Two new mutations in exon 3 of the NDP gene: S73X and S101F associated with severe and less severe ocular phenotype, respectivelyJ L Walker, J Dixon, C R Fenton, et al.
Nature Genetics|June 1, 1992
Isolation and characterization of a candidate gene for Norrie diseaseZ Y Chen, R W Hendriks, M A Jobling, et al.
Human Molecular Genetics|June 1, 1992
Characterization of a YAC containing part or all of the Norrie disease locusZ Y Chen, K B Sims, M Coleman, et al.
Human Genetics|April 1, 1990
A locus for X-linked congenital stationary night blindness is located on the proximal portion of the short arm of the X chromosomeN T Bech-Hansen, L L Field, A M Schramm, et al.
Human Genetics|December 1, 1991
Analysis of X-chromosome inactivation and presumptive expression of the Wiskott-Aldrich syndrome (WAS) gene in hematopoietic cell lineages of a thrombocytopenic carrier female of WASL D Notarangelo, O Parolini, F Porta, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Mapping the X chromosome breakpoint in two papillary renal cell carcinoma cell lines with a t(X;1)(p11.2;q21.2) and the first report of a female caseJ M Shipley, S Birdsall, J Clark, et al.
Human Genetics|May 1, 1992
Wiskott-Aldrich syndrome carrier detection with the hypervariable marker M27 betaG de Saint Basile, L D Notarangelo, C Bonaiti-Pellié, et al.
Pageof 14