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Indian Journal of Human Genetics|September 11, 2013
Sclerosterosis (Truswell-Hansen disease)S Deepak Amalnath, M VivekanandanIndian Journal of Human Genetics|August 1, 2013
The determination of Q192R polymorphism of paraoxonase 1 by using non-toxic substrate p-nitrophenylacetateM R Mogarekar, Seema S ChawhanIndian Journal of Human Genetics|August 1, 2013
A novel deletion cluster at 13q14.2-q21.33 in an 80-year man with late onset leukemia: Clinical and molecular findingsKiran Kumar, Sujit Maiti, Christina A Castellani, et al.Indian Journal of Human Genetics|December 17, 2013
Population based family history analysis of Brahmins in a small town in India for the prevalence of type-2 diabetes mellitusArun V Panat, Dilip A Kulkarni, Ravindra B GhooiIndian Journal of Human Genetics|December 17, 2013
Mosaic double aneuploidy: Down syndrome and XYYMayur Parihar, Beena Koshy, Vivi Miriam SrivastavaIndian Journal of Human Genetics|February 6, 2014
Protein tyrosine phosphatase non-receptor type 22 gene polymorphism C1858T is not associated with leprosy in Azerbaijan, Northwest IranMohammad Reza Aliparasti, Shohreh Almasi, Jafar Majidi, et al.Indian Journal of Human Genetics|February 6, 2014
Genetic polymorphisms of estrogen receptor alpha and catechol-O-methyltransferase genes in Turkish patients with familial prostate carcinomaAyfer Pazarbasi, M Bertan Yilmaz, Davut Alptekin, et al.Indian Journal of Human Genetics|February 6, 2014
Chromosomal abnormalities in couples with repeated fetal loss: An Indian retrospective studyFrenny J Sheth, Thomas Liehr, Pritti Kumari, et al.Indian Journal of Human Genetics|February 6, 2014
Mutational identification of fibroblast growth factor receptor 1 and fibroblast growth factor receptor 2 genes in craniosynostosis in Indian populationRajeev Kumar Pandey, Minu Bajpai, Abid Ali, et al.Pageof 35