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Journal of Chromatography. A
|
August 28, 2001
Analysis of dopamine D4 receptor gene polymorphism using microchip electrophoresis
C Barta, Z Ronai, Z Nemoda, et al.
Electrophoresis
|
May 19, 2001
Genotyping the -521C/T functional polymorphism in the promoter region of dopamine D4 receptor (DRD4) gene
Z Ronai, C Barta, A Guttman, et al.
Radiology
|
June 1, 1985
ECG-synchronized cardiac MR imaging: method and evaluation
P Lanzer, C Barta, E H Botvinick, et al.
Fetal Diagnosis and Therapy
|
June 16, 2001
Prenatal diagnosis of steroid 21-hydroxylase deficiency by allele-specific amplification
M Theodoropoulou, C Barta, M Szoke, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 15, 1999
Screening for mutations of 21-hydroxylase gene in Hungarian patients with congenital adrenal hyperplasia
A Ferenczi, M Garami, E Kiss, et al.
Molecular Psychiatry
|
June 25, 2008
The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase
N Mukherjee, K K Kidd, A J Pakstis, et al.
Molecular Psychiatry
|
November 16, 2011
Replication of association between a SLITRK1 haplotype and Tourette Syndrome in a large sample of families
I Karagiannidis, R Rizzo, Z Tarnok, et al.
Genes, Brain, and Behavior
|
March 23, 2012
Evaluation of the LIM homeobox genes LHX6 and LHX8 as candidates for Tourette syndrome
P Paschou, E Stylianopoulou, I Karagiannidis, et al.
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of 2
Search research articles
Search
Showing results (11-20 of 18) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 18 results.
Journal of Chromatography. A
|
August 28, 2001
Analysis of dopamine D4 receptor gene polymorphism using microchip electrophoresis
C Barta, Z Ronai, Z Nemoda, et al.
Electrophoresis
|
May 19, 2001
Genotyping the -521C/T functional polymorphism in the promoter region of dopamine D4 receptor (DRD4) gene
Z Ronai, C Barta, A Guttman, et al.
Radiology
|
June 1, 1985
ECG-synchronized cardiac MR imaging: method and evaluation
P Lanzer, C Barta, E H Botvinick, et al.
Fetal Diagnosis and Therapy
|
June 16, 2001
Prenatal diagnosis of steroid 21-hydroxylase deficiency by allele-specific amplification
M Theodoropoulou, C Barta, M Szoke, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 15, 1999
Screening for mutations of 21-hydroxylase gene in Hungarian patients with congenital adrenal hyperplasia
A Ferenczi, M Garami, E Kiss, et al.
Molecular Psychiatry
|
June 25, 2008
The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase
N Mukherjee, K K Kidd, A J Pakstis, et al.
Molecular Psychiatry
|
November 16, 2011
Replication of association between a SLITRK1 haplotype and Tourette Syndrome in a large sample of families
I Karagiannidis, R Rizzo, Z Tarnok, et al.
Genes, Brain, and Behavior
|
March 23, 2012
Evaluation of the LIM homeobox genes LHX6 and LHX8 as candidates for Tourette syndrome
P Paschou, E Stylianopoulou, I Karagiannidis, et al.
Page
of 2