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Showing results (171-180 of 270) with videos related to

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Science (New York, N.Y.)|February 7, 1998
A potassium channel mutation in neonatal human epilepsyC Biervert, B C Schroeder, C Kubisch, et al.
American Journal of Human Genetics|April 1, 1993
Pseudoautosomal marker DXYS20 and manic depressionM M Nöthen, S Cichon, J Erdmann, et al.
Molecular Psychiatry|March 13, 2001
Association study of the low-activity allele of catechol-O-methyltransferase and alcoholism using a family-based approachT Wang, P Franke, H Neidt, et al.
American Journal of Medical Genetics|June 27, 2001
Nonreplication of association between mu-opioid-receptor gene (OPRM1) A118G polymorphism and substance dependenceP Franke, T Wang, M M Nöthen, et al.
Human Genetics|March 1, 1991
Genotype-phenotype relationship in various degrees of arylsulfatase A deficiencyJ Kappler, P Leinekugel, E Conzelmann, et al.
Molecular Psychiatry|February 16, 2000
DRD4 exon III VNTR polymorphism-susceptibility factor for heroin dependence? Results of a case-control and a family-based association approachP Franke, M M Nöthen, T Wang, et al.
American Journal of Human Genetics|June 19, 2001
Variant 1859G-->A (Arg620Gln) of the "hairless" gene: absence of association with papular atrichia or androgenic alopeciaA M Hillmer, R Kruse, R C Betz, et al.
Molecular Psychiatry|March 10, 1998
Systematic mutation screening and association study of the A1 and A2a adenosine receptor genes in panic disorder suggest a contribution of the A2a gene to the development of diseaseJ Deckert, M M Nöthen, P Franke, et al.
American Journal of Human Genetics|June 23, 1998
Evidence for linkage of spelling disability to chromosome 15G Schulte-Körne, T Grimm, M M Nöthen, et al.
American Journal of Medical Genetics|April 24, 1995
Linkage studies of bipolar disorder in the region of the Darier's disease gene on chromosome 12q23-24.1E Dawson, E Parfitt, Q Roberts, et al.
Pageof 27

Showing results (171-180 of 270) with videos related to

Sort By:
Pageof 27
Science (New York, N.Y.)|February 7, 1998
A potassium channel mutation in neonatal human epilepsyC Biervert, B C Schroeder, C Kubisch, et al.
American Journal of Human Genetics|April 1, 1993
Pseudoautosomal marker DXYS20 and manic depressionM M Nöthen, S Cichon, J Erdmann, et al.
Molecular Psychiatry|March 13, 2001
Association study of the low-activity allele of catechol-O-methyltransferase and alcoholism using a family-based approachT Wang, P Franke, H Neidt, et al.
American Journal of Medical Genetics|June 27, 2001
Nonreplication of association between mu-opioid-receptor gene (OPRM1) A118G polymorphism and substance dependenceP Franke, T Wang, M M Nöthen, et al.
Human Genetics|March 1, 1991
Genotype-phenotype relationship in various degrees of arylsulfatase A deficiencyJ Kappler, P Leinekugel, E Conzelmann, et al.
Molecular Psychiatry|February 16, 2000
DRD4 exon III VNTR polymorphism-susceptibility factor for heroin dependence? Results of a case-control and a family-based association approachP Franke, M M Nöthen, T Wang, et al.
American Journal of Human Genetics|June 19, 2001
Variant 1859G-->A (Arg620Gln) of the "hairless" gene: absence of association with papular atrichia or androgenic alopeciaA M Hillmer, R Kruse, R C Betz, et al.
Molecular Psychiatry|March 10, 1998
Systematic mutation screening and association study of the A1 and A2a adenosine receptor genes in panic disorder suggest a contribution of the A2a gene to the development of diseaseJ Deckert, M M Nöthen, P Franke, et al.
American Journal of Human Genetics|June 23, 1998
Evidence for linkage of spelling disability to chromosome 15G Schulte-Körne, T Grimm, M M Nöthen, et al.
American Journal of Medical Genetics|April 24, 1995
Linkage studies of bipolar disorder in the region of the Darier's disease gene on chromosome 12q23-24.1E Dawson, E Parfitt, Q Roberts, et al.
Pageof 27