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Journal of Genetics|September 24, 2019
In silico analysis of the structural and functional implications of SLC19A1 R27H polymorphismShaik Mohammad Naushad, Akella Radha Rama Devi, Tajamul Hussain, et al.
Genomics & Informatics|October 12, 2021
Molecular insights into the role of genetic determinants of congenital hypothyroidismYedukondalu Kollati, Radha Rama Devi Akella, Shaik Mohammad Naushad, et al.
Psychiatric Genetics|May 15, 2009
Aberrations in folate metabolic pathway and altered susceptibility to autismNaushad Shaik Mohammad, Jamal Md Nurul Jain, Krishna Prasad Chintakindi, et al.
Journal of Genetics|January 12, 2018
Neuro-fuzzy model of homocysteine metabolismShaik Mohammad Naushad, Akella Radha Rama Devi, Sriraman Nivetha, et al.
Journal of Pediatric Genetics|May 8, 2019
Acute Gaucher Disease-Like Condition in an Indian Infant with a Novel Biallelic Mutation in the Prosaposin GeneAkella Radha Rama Devi, Srilatha Kadali, Ananthaneni Radhika, et al.
Andrologia|July 16, 2010
Role of glutathione S-transferase Mu-1 (GSTM1) polymorphism in oligospermic infertile malesG Tirumala Vani, N Mukesh, B Siva Prasad, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 30, 2009
Association of CYP1A1*2A polymorphism with male infertility in Indian populationGudimella Tirumala Vani, Navgire Mukesh, Badabagni Siva Prasad, et al.
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