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Human Molecular Genetics
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September 16, 1998
Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia
S Cichon, M Anker, I R Vogt, et al.
American Journal of Medical Genetics
|
May 30, 2001
Caught in the trio trap? Potential selection bias inherent to association studies using parent-offspring trios
T G Schulze, D J Müller, H Krauss, et al.
Molecular Psychiatry
|
February 18, 2004
Examination of G72 and D-amino-acid oxidase as genetic risk factors for schizophrenia and bipolar affective disorder
J Schumacher, R Abon Jamra, J Freudenberg, et al.
American Journal of Medical Genetics
|
July 14, 2000
Investigation of the human serotonin 6 [5-HT6] receptor gene in bipolar affective disorder and schizophrenia
I R Vogt, D Shimron-Abarbanell, H Neidt, et al.
Human Molecular Genetics
|
March 11, 1999
Excess of high activity monoamine oxidase A gene promoter alleles in female patients with panic disorder
J Deckert, M Catalano, Y V Syagailo, et al.
Molecular Psychiatry
|
October 13, 2004
Investigation of the DAOA/G30 locus in panic disorder
J Schumacher, R Abou Jamra, T Becker, et al.
American Journal of Medical Genetics
|
August 10, 2001
Lack of association between a functional polymorphism of the cytochrome P450 1A2 (CYP1A2) gene and tardive dyskinesia in schizophrenia
T G Schulze, J Schumacher, D J Müller, et al.
Molecular Psychiatry
|
December 18, 2008
Two variants in Ankyrin 3 (ANK3) are independent genetic risk factors for bipolar disorder
T G Schulze, S D Detera-Wadleigh, N Akula, et al.
Psychiatric Genetics
|
March 4, 2000
hSKCa3: no association of the polymorphic CAG repeat with bipolar affective disorder and schizophrenia
T Rohrmeier, A Putzhammer, A Schoeler, et al.
Journal of Medical Genetics
|
September 18, 2007
High proportion of large genomic deletions and a genotype phenotype update in 80 unrelated families with juvenile polyposis syndrome
S Aretz, D Stienen, S Uhlhaas, et al.
Page
of 27
Search research articles
Search
Showing results (241-250 of 270) with videos related to
Sort By:
Page
of 27
Human Molecular Genetics
|
September 16, 1998
Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia
S Cichon, M Anker, I R Vogt, et al.
American Journal of Medical Genetics
|
May 30, 2001
Caught in the trio trap? Potential selection bias inherent to association studies using parent-offspring trios
T G Schulze, D J Müller, H Krauss, et al.
Molecular Psychiatry
|
February 18, 2004
Examination of G72 and D-amino-acid oxidase as genetic risk factors for schizophrenia and bipolar affective disorder
J Schumacher, R Abon Jamra, J Freudenberg, et al.
American Journal of Medical Genetics
|
July 14, 2000
Investigation of the human serotonin 6 [5-HT6] receptor gene in bipolar affective disorder and schizophrenia
I R Vogt, D Shimron-Abarbanell, H Neidt, et al.
Human Molecular Genetics
|
March 11, 1999
Excess of high activity monoamine oxidase A gene promoter alleles in female patients with panic disorder
J Deckert, M Catalano, Y V Syagailo, et al.
Molecular Psychiatry
|
October 13, 2004
Investigation of the DAOA/G30 locus in panic disorder
J Schumacher, R Abou Jamra, T Becker, et al.
American Journal of Medical Genetics
|
August 10, 2001
Lack of association between a functional polymorphism of the cytochrome P450 1A2 (CYP1A2) gene and tardive dyskinesia in schizophrenia
T G Schulze, J Schumacher, D J Müller, et al.
Molecular Psychiatry
|
December 18, 2008
Two variants in Ankyrin 3 (ANK3) are independent genetic risk factors for bipolar disorder
T G Schulze, S D Detera-Wadleigh, N Akula, et al.
Psychiatric Genetics
|
March 4, 2000
hSKCa3: no association of the polymorphic CAG repeat with bipolar affective disorder and schizophrenia
T Rohrmeier, A Putzhammer, A Schoeler, et al.
Journal of Medical Genetics
|
September 18, 2007
High proportion of large genomic deletions and a genotype phenotype update in 80 unrelated families with juvenile polyposis syndrome
S Aretz, D Stienen, S Uhlhaas, et al.
Page
of 27