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C Barta

Showing results (11-20 of 18) with videos related to

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Journal of Chromatography. A|August 28, 2001
Analysis of dopamine D4 receptor gene polymorphism using microchip electrophoresisC 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) geneZ Ronai, C Barta, A Guttman, et al.
Radiology|June 1, 1985
ECG-synchronized cardiac MR imaging: method and evaluationP 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 amplificationM 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 hyperplasiaA 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-methyltransferaseN 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 familiesI 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 syndromeP Paschou, E Stylianopoulou, I Karagiannidis, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 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 electrophoresisC 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) geneZ Ronai, C Barta, A Guttman, et al.
Radiology|June 1, 1985
ECG-synchronized cardiac MR imaging: method and evaluationP 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 amplificationM 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 hyperplasiaA 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-methyltransferaseN 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 familiesI 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 syndromeP Paschou, E Stylianopoulou, I Karagiannidis, et al.
Pageof 2