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Indian Journal of Human Genetics|December 17, 2013
A novel ABCB11 mutation in an Iranian girl with progressive familial intrahepatic cholestasisSassan Saber, Reza Vazifehmand, Iman Bagherizadeh, et al.Indian Journal of Human Genetics|December 17, 2013
Novel three missense mutations observed in Von Hippel-Lindau gene in a patient reported with renal cell carcinomaPasupuleti Santhosh Kumar, Katari Venkatesh, Lokanathan Srikanth, et al.Indian Journal of Human Genetics|October 30, 2010
Genetic variations of β-MYH7 in hypertrophic cardiomyopathy and dilated cardiomyopathyReena Tanjore, Advithi Rangaraju, Shivani Vadapalli, et al.Indian Journal of Human Genetics|November 20, 2010
A new recurring chromosome 13 abnormality in two older patients with de novo acute myeloid leukemia: An Indian experienceP J Trivedi, P S Patel, M M Brahmbhatt, et al.Indian Journal of Human Genetics|January 6, 2011
Pharmacogenomics of pediatric asthmaSarika Gupta, Shally AwasthiIndian Journal of Human Genetics|January 6, 2011
Bone age is the best predictor of growth response to recombinant human growth hormone in Turner's syndromeNagwa Abdallah Ismail, Nermeen Salah Eldin Metwaly, Fatma Ahmed El-Moguy, et al.Indian Journal of Human Genetics|January 6, 2011
Genetic assessment of serological and biochemical markers in Bharia tribe of Chhindwara district of Madhya PradeshRuchira Chaudhary, Gunjan SharmaIndian Journal of Human Genetics|January 6, 2011
The NQO1 allelic frequency in hindu population of central India varies from that of other Asian populationsSher S Parihar, U K ChauhanIndian Journal of Human Genetics|January 6, 2011
Molecular analysis of human leukocyte antigen class I and class II allele frequencies and haplotype distribution in Pakistani populationT Moatter, M Aban, S Tabassum, et al.Indian Journal of Human Genetics|January 6, 2011
Oculo-facio-cardio-dental syndrome in a girl and her motherSudha Rudrappa, Rajendra Kumar, G S KumarPageof 35