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Molecular and Cellular Probes
|
September 6, 2000
Mutation screening of the chromosome 8q24.3-human activity-regulated cytoskeleton-associated gene (ARC) in idiopathic generalized epilepsy
K Haug, J Kremerskothen, K Hallmann, et al.
Gut
|
March 15, 2001
Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis? Experience from 680 FAP families
W Friedl, R Caspari, M Sengteller, et al.
Behavior Genetics
|
March 1, 1996
Assessing the statistical power to detect linkage in a sample of 51 bipolar affective disorder pedigrees
L C Lim, N Craddock, M Owen, et al.
Annals of Human Genetics
|
October 14, 2006
Interrelationship and familiality of dyslexia related quantitative measures
G Schulte-Körne, A Ziegler, W Deimel, et al.
Molecular Psychiatry
|
October 17, 2007
Genetic variation of the FAT gene at 4q35 is associated with bipolar affective disorder
R Abou Jamra, T Becker, A Georgi, et al.
American Journal of Medical Genetics
|
July 18, 2000
Association study of the tryptophan hydroxylase gene and bipolar affective disorder using family-based internal controls
M Rietschel, A Schorr, M Albus, et al.
Human Genetics
|
May 1, 1996
Systematic screening for mutations in the human serotonin-2A (5-HT2A) receptor gene: identification of two naturally occurring receptor variants and association analysis in schizophrenia
J Erdmann, D Shimron-Abarbanell, M Rietschel, et al.
American Journal of Medical Genetics
|
July 26, 1996
Systematic screening for mutations in the 5'-regulatory region of the human dopamine D1 receptor (DRD1) gene in patients with schizophrenia and bipolar affective disorder
S Cichon, M M Nöthen, G Stöber, et al.
American Journal of Human Genetics
|
June 23, 1998
Muir-Torre phenotype has a frequency of DNA mismatch-repair-gene mutations similar to that in hereditary nonpolyposis colorectal cancer families defined by the Amsterdam criteria
R Kruse, A Rütten, C Lamberti, et al.
American Journal of Human Genetics
|
April 16, 1998
A gene for universal congenital alopecia maps to chromosome 8p21-22
M M Nöthen, S Cichon, I R Vogt, et al.
Page
of 27
Search research articles
Search
Showing results (221-230 of 270) with videos related to
Sort By:
Page
of 27
Molecular and Cellular Probes
|
September 6, 2000
Mutation screening of the chromosome 8q24.3-human activity-regulated cytoskeleton-associated gene (ARC) in idiopathic generalized epilepsy
K Haug, J Kremerskothen, K Hallmann, et al.
Gut
|
March 15, 2001
Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis? Experience from 680 FAP families
W Friedl, R Caspari, M Sengteller, et al.
Behavior Genetics
|
March 1, 1996
Assessing the statistical power to detect linkage in a sample of 51 bipolar affective disorder pedigrees
L C Lim, N Craddock, M Owen, et al.
Annals of Human Genetics
|
October 14, 2006
Interrelationship and familiality of dyslexia related quantitative measures
G Schulte-Körne, A Ziegler, W Deimel, et al.
Molecular Psychiatry
|
October 17, 2007
Genetic variation of the FAT gene at 4q35 is associated with bipolar affective disorder
R Abou Jamra, T Becker, A Georgi, et al.
American Journal of Medical Genetics
|
July 18, 2000
Association study of the tryptophan hydroxylase gene and bipolar affective disorder using family-based internal controls
M Rietschel, A Schorr, M Albus, et al.
Human Genetics
|
May 1, 1996
Systematic screening for mutations in the human serotonin-2A (5-HT2A) receptor gene: identification of two naturally occurring receptor variants and association analysis in schizophrenia
J Erdmann, D Shimron-Abarbanell, M Rietschel, et al.
American Journal of Medical Genetics
|
July 26, 1996
Systematic screening for mutations in the 5'-regulatory region of the human dopamine D1 receptor (DRD1) gene in patients with schizophrenia and bipolar affective disorder
S Cichon, M M Nöthen, G Stöber, et al.
American Journal of Human Genetics
|
June 23, 1998
Muir-Torre phenotype has a frequency of DNA mismatch-repair-gene mutations similar to that in hereditary nonpolyposis colorectal cancer families defined by the Amsterdam criteria
R Kruse, A Rütten, C Lamberti, et al.
American Journal of Human Genetics
|
April 16, 1998
A gene for universal congenital alopecia maps to chromosome 8p21-22
M M Nöthen, S Cichon, I R Vogt, et al.
Page
of 27