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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 LaSalleHuman 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 GragertHuman 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 RichHuman Genetics|August 1, 1991
Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13A L Pettigrew, F Greenberg, C T Caskey, et al.Human Genetics|August 1, 1991
Mutation analysis of glucose-6-phosphate dehydrogenase (G6PD) variants in Costa RicaE Beutler, W Kuhl, G F Sáenz, et al.Pageof 959