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Indian Journal of Human Genetics|August 1, 2013
Tuberous sclerosis with rhabdomyomaV Ajay, Vikram Singhal, Vardhelli Venkateshwarlu, et al.Indian Journal of Human Genetics|August 1, 2013
Short stature and an interesting associationLatha Magatha Sneha, Kishore Thanasegarapandian, Venkataraman Paramasivam, et al.Indian Journal of Human Genetics|August 1, 2013
A case of bilateral tibial hemimelia type VIIaSelvakumar Chinnakkannan, Rashmi Ranjan Das, K Rughmini, et al.Indian Journal of Human Genetics|February 6, 2014
Deoxyribonucleic acid damage study in primary amenorrhea by comet assay and karyotypingSarah Ramamurthy, Parkash Chand, Latha Chaturvedula, et al.Indian Journal of Human Genetics|February 6, 2014
Mutation analysis of mitogen activated protein kinase 1 gene in Indian cases of 46,XY disorder of sex developmentDhanjit Kumar Das, Subodh G Rahate, Bhakti P Mehta, et al.Indian Journal of Human Genetics|February 6, 2014
Molecular characterization in a case of isolated growth hormone deficiency and further prenatal diagnosis of an unborn siblingRuchi Nadar, Kavita Khatod, Nikhil Phadke, et al.Indian Journal of Human Genetics|February 6, 2014
Double heterozygous hemoglobin Q India/hemoglobin D Punjab hemoglobinopathy: Report of two rare casesDeepti Mutreja, Seema Tyagi, Narender Tejwani, et al.Indian Journal of Human Genetics|February 6, 2014
Deoxyribonucleic acid repair gene X-ray repair cross-complementing group 1 polymorphisms and non-carcinogenic disease risk in different populations: A meta-analysisBagher Larijani, Javad Mohammadi Asl, Abbas Keshtkar, et al.Indian Journal of Human Genetics|December 17, 2013
Hemoglobin E disorder: Newborn screening programViroj WiwanitkitIndian Journal of Human Genetics|December 17, 2013
Linkage study of DFNB3 responsible for hearing loss in humanAkhtar Ali, Masroor E Babar, Saeeda Kalsoom, et al.Pageof 35