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Annals of Human Genetics|August 14, 2003
Saturation of the 5q31-q33 candidate region for coeliac diseaseS Percopo, M-C Babron, M Whalen, et al.Annals of Human Genetics|May 1, 1987
Electrophoretic and immunological analysis of human glutathione S-transferase isozymesT Suzuki, M Coggan, D C Shaw, et al.Annals of Human Genetics|June 14, 2019
Genetic history of the population of CretePetros Drineas, Fotis Tsetsos, Anna Plantinga, et al.Annals of Human Genetics|June 14, 2019
Novel mutation in the DSG1 gene causes autosomal-dominant striate palmoplantar keratoderma in a large Syrian familyBatoul Abi Zamer, Mona Mahfood, Batoul Saleh, et al.Annals of Human Genetics|April 13, 2019
A novel SLC12A1 mutation in Bedouin kindred with antenatal Bartter syndrome type IDaniel Halperin, Vadim Dolgin, Michael Geylis, et al.Annals of Human Genetics|May 19, 2018
Analysis of type 2 diabetes and obesity genetic variants in Mexican Pima Indians: Marked allelic differentiation among Amerindians at HLAWen-Chi Hsueh, Peter H Bennett, Julian Esparza-Romero, et al.Annals of Human Genetics|July 25, 2018
Genetic susceptibility of glutathione S-transferase genes (GSTM1/T1 and P1) to coronary artery disease in Asian IndiansJ S Bhatti, R Vijayvergiya, B Singh, et al.Annals of Human Genetics|July 25, 2018
The association of LRP6 rs2302685 (V1062I) polymorphism with the risk of hyperlipidemia in Iranian children and adolescentsNima Montazeri-Najafabady, Mohammad Hossein Dabbaghmanesh, Rajeeh Mohammadian AmiriAnnals of Human Genetics|July 25, 2018
Exome sequencing revealed a novel deletion in the ERCC8 gene in an Iranian family with Cockayne syndromeJ Mohammadi-Asl, M Hajjari, M Tahmasebi Birgani, et al.Pageof 231