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Journal of Human Genetics|June 4, 2010
Diagnosis and fine mapping of a deletion in distal 11q in two Chinese patients with developmental delayTaoyun Ji, Ye Wu, Huifang Wang, et al.Journal of Human Genetics|June 4, 2010
Common genetic variants in pre-microRNAs and risk of gallbladder cancer in North Indian populationKshitij Srivastava, Anvesha Srivastava, Balraj MittalJournal of Human Genetics|August 27, 2010
Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populationsNejat Mahdieh, Bahareh Rabbani, Susan Wiley, et al.Journal of Human Genetics|July 30, 2010
Genome-wide pathway analysis implicates intracellular transmembrane protein transport in Alzheimer diseaseMun-Gwan Hong, Andrey Alexeyenko, Jean-Charles Lambert, et al.Journal of Human Genetics|June 11, 2010
MDM2 SNP309 and p53 Arg72Pro in cutaneous melanoma: association between SNP309 GG genotype and tumor Breslow thicknessMario Capasso, Fabrizio Ayala, Rosa Anna Avvisati, et al.Journal of Human Genetics|September 10, 2010
Contemporary retrotransposition of a novel non-coding gene induces exon-skipping in dystrophin mRNAHiroyuki Awano, Rusdy Ghazali Malueka, Mariko Yagi, et al.Journal of Human Genetics|October 29, 2010
The ENPP1 K121Q polymorphism is not associated with type 2 diabetes or obesity in the Chinese Han populationTeng Zhao, Zhe Liu, Di Zhang, et al.Journal of Human Genetics|November 19, 2010
A new c.1621 C > G, p.R541G lamin A/C mutation in a family with DCM and regional wall motion abnormalities (akinesis/dyskinesis): genotype-phenotype correlationLukasz A Małek, Sarah Labib, Lukasz Mazurkiewicz, et al.Journal of Human Genetics|December 3, 2010
An isoform of the severe encephalopathy-related CDKL5 gene, including a novel exon with extremely high sequence conservation, is specifically expressed in brainYann Fichou, Juliette Nectoux, Nadia Bahi-Buisson, et al.Journal of Human Genetics|November 26, 2010
Cyclin D1 rare variants in UK multiple adenoma and early-onset colorectal cancer patientsCarolina Bonilla, Jérémie H Lefèvre, Bruce Winney, et al.Pageof 351