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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.
Molecular Psychiatry
|
March 12, 2008
A genome-wide association study in 574 schizophrenia trios using DNA pooling
G Kirov, I Zaharieva, L Georgieva, et al.
Psychiatry Research
|
March 1, 1993
A serine to glycine substitution at position 9 in the extracellular N-terminal part of the dopamine D3 receptor protein: no role in the genetic predisposition to bipolar affective disorder
M Rietschel, M M Nöthen, L Lannfelt, et al.
American Journal of Human Genetics
|
July 6, 2000
Localization of a gene for syndactyly type 1 to chromosome 2q34-q36
K Bosse, R C Betz, Y A Lee, et al.
American Journal of Medical Genetics
|
October 9, 1995
Systematic screening for mutations in the promoter and the coding region of the 5-HT1A gene
J Erdmann, D Shimron-Abarbanell, S Cichon, et al.
Psychiatric Genetics
|
January 1, 1995
Identification of two novel polymorphisms and a rare deletion variant in the human dopamine D4 receptor gene
S Cichon, M M Nöthen, M Catalano, et al.
American Journal of Medical Genetics
|
September 15, 1994
Association analysis of the dopamine D2 receptor gene in Tourette's syndrome using the haplotype relative risk method
M M Nöthen, J Hebebrand, M Knapp, et al.
Journal of Endocrinological Investigation
|
May 24, 2003
Incidence of thyroid cancer in the selected areas of iodine deficiency in Poland
Z Szybiński, B Huszno, B Zemla, et al.
American Journal of Medical Genetics
|
April 17, 1999
Tourette syndrome and the norepinephrine transporter gene: results of a systematic mutation screening
G Stöber, J Hebebrand, S Cichon, et al.
Molecular Psychiatry
|
March 11, 2015
Evaluating historical candidate genes for schizophrenia
M S Farrell, T Werge, P Sklar, et al.
Page
of 12
Search research articles
Search
Showing results (31-40 of 112) with videos related to
Sort By:
Page
of 12
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.
Molecular Psychiatry
|
March 12, 2008
A genome-wide association study in 574 schizophrenia trios using DNA pooling
G Kirov, I Zaharieva, L Georgieva, et al.
Psychiatry Research
|
March 1, 1993
A serine to glycine substitution at position 9 in the extracellular N-terminal part of the dopamine D3 receptor protein: no role in the genetic predisposition to bipolar affective disorder
M Rietschel, M M Nöthen, L Lannfelt, et al.
American Journal of Human Genetics
|
July 6, 2000
Localization of a gene for syndactyly type 1 to chromosome 2q34-q36
K Bosse, R C Betz, Y A Lee, et al.
American Journal of Medical Genetics
|
October 9, 1995
Systematic screening for mutations in the promoter and the coding region of the 5-HT1A gene
J Erdmann, D Shimron-Abarbanell, S Cichon, et al.
Psychiatric Genetics
|
January 1, 1995
Identification of two novel polymorphisms and a rare deletion variant in the human dopamine D4 receptor gene
S Cichon, M M Nöthen, M Catalano, et al.
American Journal of Medical Genetics
|
September 15, 1994
Association analysis of the dopamine D2 receptor gene in Tourette's syndrome using the haplotype relative risk method
M M Nöthen, J Hebebrand, M Knapp, et al.
Journal of Endocrinological Investigation
|
May 24, 2003
Incidence of thyroid cancer in the selected areas of iodine deficiency in Poland
Z Szybiński, B Huszno, B Zemla, et al.
American Journal of Medical Genetics
|
April 17, 1999
Tourette syndrome and the norepinephrine transporter gene: results of a systematic mutation screening
G Stöber, J Hebebrand, S Cichon, et al.
Molecular Psychiatry
|
March 11, 2015
Evaluating historical candidate genes for schizophrenia
M S Farrell, T Werge, P Sklar, et al.
Page
of 12