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Indian Journal of Human Genetics|March 20, 2010
The CTLA4 -819 C/T and +49 A/G dimorphisms are associated with Type 1 diabetes in Egyptian childrenHatem Mohamed Saleh, Nestor Rohowsky, Michael LeskiIndian Journal of Human Genetics|March 20, 2010
Bloom's syndrome in a 12-year-old Iranian girlNaeimeh Tayebi, Hossain KhodaeiIndian Journal of Human Genetics|June 25, 2014
Genes and oral cancerSunit Kumar Jurel, Durga Shanker Gupta, Raghuwar D Singh, et al.Indian Journal of Human Genetics|June 25, 2014
Neurotransmitters in alcoholism: A review of neurobiological and genetic studiesNiladri BanerjeeIndian Journal of Human Genetics|June 25, 2014
Association study of the ABCC8 gene variants with type 2 diabetes in south IndiansRadha Venkatesan, Dhanasekaran Bodhini, Nagarajan Narayani, et al.Indian Journal of Human Genetics|June 25, 2014
Paraoxonase1, its Q192R polymorphism and HDL-cholesterol in relation to intensive cardiac care unit stay in ischemic heart diseaseMahesh Harishchandra Hampe, Mukund Ramchandra MogarekarIndian Journal of Human Genetics|June 25, 2014
Raine syndromeB Vishwanath, K Srinivasa, M Veera ShankarIndian Journal of Human Genetics|June 25, 2014
Poland syndromeChandra Madhur Sharma, Shrawan Kumar, Manoj K Meghwani, et al.Indian Journal of Human Genetics|January 6, 2011
Methionine synthase polymorphisms (MTR 2756 A>G and MTR 2758 C>G) frequencies and distribution in the Jordanian population and their correlation with neural tube defects in the population of the northern part of JordanHelmi Yousif Al FarraIndian Journal of Human Genetics|January 6, 2011
Clinical, hematologic and molecular variability of sickle cell-β thalassemia in western IndiaMalay B Mukherjee, Anita H Nadkarni, Ajit C Gorakshakar, et al.Pageof 35