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The American Journal of Psychiatry
|
May 1, 1997
Lack of evidence for allelic association between personality traits and the dopamine D4 receptor gene polymorphisms
E G Jönsson, M M Nöthen, J P Gustavsson, et al.
European Child & Adolescent Psychiatry
|
January 19, 2000
Genetic linkage analysis with dyslexia: evidence for linkage of spelling disability to chromosome 15
M M Nöthen, G Schulte-Körne, T Grimm, et al.
Pharmacogenetics
|
August 16, 2001
Association between the 5' UTR variant C178T of the serotonin receptor gene HTR3A and bipolar affective disorder
B Niesler, T Flohr, M M Nöthen, et al.
Clinical Neuropharmacology
|
January 1, 1992
Association and linkage studies in bipolar affective disorder
M Lanczik, M Nöthen, J Körner, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology
|
November 1, 1996
Efficacy and side-effects of clozapine: testing for association with allelic variation in the dopamine D4 receptor gene
M Rietschel, D Naber, H Oberländer, et al.
The British Journal of Dermatology
|
November 9, 2000
A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
S Cichon, R Kruse, A M Hillmer, et al.
The American Journal of Psychiatry
|
February 1, 1992
Lack of association between dopamine D1 and D2 receptor genes and bipolar affective disorder
M M Nöthen, J Erdmann, J Körner, et al.
American Journal of Medical Genetics
|
September 15, 1994
No evidence of association between dopamine D4 receptor variants and bipolar affective disorder
L C Lim, M M Nöthen, J Körner, et al.
American Journal of Human Genetics
|
March 1, 1993
Compound heterozygosity for metachromatic leukodystrophy and arylsulfatase A pseudodeficiency alleles is not associated with progressive neurological disease
J M Penzien, J Kappler, N Herschkowitz, et al.
The British Journal of Dermatology
|
April 23, 2002
The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approach
A M Hillmer, R Kruse, F Macciardi, et al.
Page
of 27
Search research articles
Search
Showing results (181-190 of 270) with videos related to
Sort By:
Page
of 27
The American Journal of Psychiatry
|
May 1, 1997
Lack of evidence for allelic association between personality traits and the dopamine D4 receptor gene polymorphisms
E G Jönsson, M M Nöthen, J P Gustavsson, et al.
European Child & Adolescent Psychiatry
|
January 19, 2000
Genetic linkage analysis with dyslexia: evidence for linkage of spelling disability to chromosome 15
M M Nöthen, G Schulte-Körne, T Grimm, et al.
Pharmacogenetics
|
August 16, 2001
Association between the 5' UTR variant C178T of the serotonin receptor gene HTR3A and bipolar affective disorder
B Niesler, T Flohr, M M Nöthen, et al.
Clinical Neuropharmacology
|
January 1, 1992
Association and linkage studies in bipolar affective disorder
M Lanczik, M Nöthen, J Körner, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology
|
November 1, 1996
Efficacy and side-effects of clozapine: testing for association with allelic variation in the dopamine D4 receptor gene
M Rietschel, D Naber, H Oberländer, et al.
The British Journal of Dermatology
|
November 9, 2000
A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
S Cichon, R Kruse, A M Hillmer, et al.
The American Journal of Psychiatry
|
February 1, 1992
Lack of association between dopamine D1 and D2 receptor genes and bipolar affective disorder
M M Nöthen, J Erdmann, J Körner, et al.
American Journal of Medical Genetics
|
September 15, 1994
No evidence of association between dopamine D4 receptor variants and bipolar affective disorder
L C Lim, M M Nöthen, J Körner, et al.
American Journal of Human Genetics
|
March 1, 1993
Compound heterozygosity for metachromatic leukodystrophy and arylsulfatase A pseudodeficiency alleles is not associated with progressive neurological disease
J M Penzien, J Kappler, N Herschkowitz, et al.
The British Journal of Dermatology
|
April 23, 2002
The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approach
A M Hillmer, R Kruse, F Macciardi, et al.
Page
of 27