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Annals of Human Genetics|March 4, 2020
Novel variant p.(Ala102Thr) in SDHB causes mitochondrial complex II deficiency: Case report and review of the literatureParneet Kaur, Suvasini Sharma, Rajagopal Kadavigere, et al.Annals of Human Genetics|November 8, 2012
Evaluating mitochondrial DNA variation in autism spectrum disordersAthena Hadjixenofontos, Michael A Schmidt, Patrice L Whitehead, et al.Annals of Human Genetics|March 20, 2015
Novel A219P mutation of hydroxymethylbilane synthase identified in a Chinese woman with acute intermittent porphyria and syndrome of inappropriate antidiuretic hormoneYingjie Li, Hua Qu, Hang Wang, et al.Annals of Human Genetics|October 1, 1988
Evidence on incest based on homozygosity. The use of multiple hypervariable probes for the probable detection or exclusion of incestJ H EdwardsAnnals of Human Genetics|June 26, 2014
Low back and common widespread pain share common genetic determinantsIda Malkin, Frances M K Williams, Genevieve LaChance, et al.Annals of Human Genetics|June 9, 2006
Incorporating serotypes into family based association studies using the MFG testS L Minassian, C G S Palmer, J A Turunen, et al.Annals of Human Genetics|June 9, 2006
The European-specific mitochondrial cluster J/T could confer an increased risk of insulin-resistance and type 2 diabetes: an analysis of the m.4216T > C and m.4917A > G variantsD Crispim, L H Canani, J L Gross, et al.Annals of Human Genetics|January 18, 2007
Haplotype structure of FSHB, the beta-subunit gene for fertility-associated follicle-stimulating hormone: possible influence of balancing selectionM Grigorova, K Rull, M LaanAnnals of Human Genetics|January 18, 2007
Heritability for plasma VEGF concentration in the Stanislas family studyHind Berrahmoune, Bernard Herbeth, John V Lamont, et al.Annals of Human Genetics|January 18, 2007
Dissecting the genetic history of São Tomé e Príncipe: a new window from Y-chromosome biallelic markersM J Trovoada, L Tavares, L Gusmão, et al.Pageof 231