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Journal of Human Genetics|February 8, 2013
3'-UTR variations and G6PD deficiencyFarahnaz Amini, Endom IsmailJournal of Human Genetics|February 15, 2013
A founder haplotype of APOE-Sendai mutation associated with lipoprotein glomerulopathyKentaro Toyota, Taeko Hashimoto, Daisuke Ogino, et al.Journal of Human Genetics|January 11, 2013
Quaternary protein modeling to predict the function of DNA variation found in human mitochondrial cytochrome c oxidaseMartin Patrick Horan, Jon N Rumbley, Richard G Melvin, et al.Journal of Human Genetics|January 11, 2013
The proportion of uniparental disomy is increased in Prader-Willi syndrome due to an advanced maternal childbearing age in KoreaSung Yoon Cho, Chang-Seok Ki, Young Bae Sohn, et al.Journal of Human Genetics|January 11, 2013
Polymorphisms in regulators of xenobiotic transport and metabolism genes PXR and CAR do not affect multiple myeloma risk: a case-control study in the context of the IMMEnSE consortiumAlessandro Martino, Juan Sainz, Rui Manuel Reis, et al.Journal of Human Genetics|April 19, 2013
A molecular genetic analysis of childhood nephrotic syndrome in a cohort of Saudi Arabian familiesMohamed H Al-Hamed, Essam Al-Sabban, Hamad Al-Mojalli, et al.Journal of Human Genetics|May 31, 2013
Tet family of 5-methylcytosine dioxygenases in mammalian developmentHongbo Zhao, Taiping ChenJournal of Human Genetics|May 31, 2013
A common and two novel GBA mutations in Thai patients with Gaucher diseaseRachaneekorn Tammachote, Siraprapa Tongkobpetch, Chalurmpon Srichomthong, et al.Journal of Human Genetics|July 19, 2013
Tracing the genomic ancestry of Peruvians reveals a major legacy of pre-Columbian ancestorsJose R Sandoval, Alberto Salazar-Granara, Oscar Acosta, et al.Journal of Human Genetics|August 30, 2013
Novel PKD1 and PKD2 mutations in Taiwanese patients with autosomal dominant polycystic kidney diseaseMing-Yang Chang, Hsiao-Mang Chen, Chang-Chyi Jenq, et al.Pageof 351