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Journal of Human Genetics|June 3, 2011
A population-based study of copy number variants and regions of homozygosity in healthy Swedish individualsShu-Mei Teo, Chee-Seng Ku, Nasheen Naidoo, et al.
Journal of Human Genetics|June 3, 2011
Molecular and clinical studies of X-linked deafness among Pakistani familiesAli M Waryah, Zubair M Ahmed, Munir A Bhinder, et al.
Journal of Human Genetics|March 18, 2011
HLA-C, CSTA and DS12346 susceptibility alleles confer over 100-fold increased risk of developing psoriasis: evidence of gene interactionYiannis Vasilopoulos, Gurdeep S Sagoo, Michael J Cork, et al.
Journal of Human Genetics|April 8, 2011
Gene-gene interactions contribute to eye colour variation in humansEwelina Pośpiech, Jolanta Draus-Barini, Tomasz Kupiec, et al.
Journal of Human Genetics|May 27, 2011
16p13.11 duplication is a risk factor for a wide spectrum of neuropsychiatric disordersArivudainambi Ramalingam, Xin-Gang Zhou, Stephanie D Fiedler, et al.
Journal of Human Genetics|May 27, 2011
Association of interleukin-1β genetic polymorphisms with cognitive performance in elderly females without dementiaDaimei Sasayama, Hiroaki Hori, Toshiya Teraishi, et al.
Journal of Human Genetics|October 21, 2011
Detection of uniparental isodisomy in autosomal recessive mitochondrial DNA depletion syndrome by high-density SNP array analysisGanka V Douglas, Joanna Wiszniewska, Mark H Lipson, et al.
Journal of Human Genetics|October 21, 2011
Mutational analysis for biotinidase deficiency of a Greek patients' cohort ascertained through expanded newborn screeningGeorgia Thodi, Elina Molou, Vassiliki Georgiou, et al.
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