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Human genetics

Showing results (231-240 of 11,262) with videos related to

Pageof 1,127
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Human Genetics|February 25, 2012
Cognitive and serum BDNF correlates of BDNF Val66Met gene polymorphism in patients with schizophrenia and normal controlsXiang Yang Zhang, Da Chun Chen, Mei Hong Xiu, et al.
Human Genetics|March 13, 2012
Coexisting mutations/polymorphisms of the long QT syndrome genes in patients with repaired Tetralogy of Fallot are associated with the risks of life-threatening eventsShuenn-Nan Chiu, Mei-Hwan Wu, Ming-Jai Su, et al.
Human Genetics|February 28, 2012
NIPA2 located in 15q11.2 is mutated in patients with childhood absence epilepsyYuwu Jiang, Yuehua Zhang, Pingping Zhang, et al.
Human Genetics|February 29, 2012
Polymorphisms in the XPG gene and risk of gastric cancer in Chinese populationsJing He, Li-Xin Qiu, Meng-Yun Wang, et al.
Human Genetics|August 30, 2008
Gender influences monoallelic expression of ATP10A in human brainAmber Hogart, Katherine A Patzel, Janine M LaSalle
Human Genetics|August 30, 2008
A germline mutation of the KIF1B beta gene on 1p36 in a family with neural and nonneural tumorsI-Tien Yeh, Romina E Lenci, Yuejuan Qin, et al.
Human Genetics|September 23, 2008
Partial AZFc deletions and duplications: clinical correlates in the Italian populationClaudia Giachini, Ilaria Laface, Elena Guarducci, et al.
Human Genetics|September 30, 2008
Re-creation of the genetic composition of a founder populationWilliam Klitz, Martin Maiers, Loren Gragert
Human Genetics|September 17, 2008
Apparent autosomal dominant keratoconus in a large Australian pedigree accounted for by digenic inheritance of two novel lociKathryn P Burdon, Douglas J Coster, Jac C Charlesworth, et al.
Human Genetics|August 1, 1991
Spinocerebellar ataxia: multipoint linkage analysis of genes associated with the disease locusP J Wilkie, L J Schut, S S Rich
Pageof 1,127

Showing results (231-240 of 11,262) with videos related to

Sort By:
Pageof 1,127
Human Genetics|February 25, 2012
Cognitive and serum BDNF correlates of BDNF Val66Met gene polymorphism in patients with schizophrenia and normal controlsXiang Yang Zhang, Da Chun Chen, Mei Hong Xiu, et al.
Human Genetics|March 13, 2012
Coexisting mutations/polymorphisms of the long QT syndrome genes in patients with repaired Tetralogy of Fallot are associated with the risks of life-threatening eventsShuenn-Nan Chiu, Mei-Hwan Wu, Ming-Jai Su, et al.
Human Genetics|February 28, 2012
NIPA2 located in 15q11.2 is mutated in patients with childhood absence epilepsyYuwu Jiang, Yuehua Zhang, Pingping Zhang, et al.
Human Genetics|February 29, 2012
Polymorphisms in the XPG gene and risk of gastric cancer in Chinese populationsJing He, Li-Xin Qiu, Meng-Yun Wang, et al.
Human Genetics|August 30, 2008
Gender influences monoallelic expression of ATP10A in human brainAmber Hogart, Katherine A Patzel, Janine M LaSalle
Human Genetics|August 30, 2008
A germline mutation of the KIF1B beta gene on 1p36 in a family with neural and nonneural tumorsI-Tien Yeh, Romina E Lenci, Yuejuan Qin, et al.
Human Genetics|September 23, 2008
Partial AZFc deletions and duplications: clinical correlates in the Italian populationClaudia Giachini, Ilaria Laface, Elena Guarducci, et al.
Human Genetics|September 30, 2008
Re-creation of the genetic composition of a founder populationWilliam Klitz, Martin Maiers, Loren Gragert
Human Genetics|September 17, 2008
Apparent autosomal dominant keratoconus in a large Australian pedigree accounted for by digenic inheritance of two novel lociKathryn P Burdon, Douglas J Coster, Jac C Charlesworth, et al.
Human Genetics|August 1, 1991
Spinocerebellar ataxia: multipoint linkage analysis of genes associated with the disease locusP J Wilkie, L J Schut, S S Rich
Pageof 1,127