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Indian Pediatrics|October 25, 2016
Ethylmalonic Encephalopathy in an Indian BoySunita Bijarnia-Mahay, Deepti Gupta, Yosuke Shigematsu, et al.
The Indian Journal of Medical Research|October 1, 1996
Improved method for study of chromosomes of chorionic villus samplesM R Chowdhury, R Mathur, K Prabhakara, et al.
Indian Pediatrics|September 1, 1996
Clinical and enzyme studies in Gaucher diseaseM Kaur, M Kabra, A Kher, et al.
Indian Journal of Pediatrics|January 1, 1991
Hormonal therapy in undescended testesM Rohatgi, D K Gupta, P S Menon, et al.
Brain & Development|September 4, 2016
RANBP2 mutation in an Indian child with recurrent acute necrotizing encephalopathyVishal Sondhi, Biswaroop Chakrabarty, Atin Kumar, et al.
The Indian Journal of Medical Research|November 18, 2011
ATR-X syndrome in two siblings with a novel mutation (c.6718C>T mutation in exon 31)Seema Thakur, Mala Ishrie, Renu Saxena, et al.
The Indian Journal of Medical Research|November 1, 1996
Karyotyping of at risk fetuses by cordocentesis in advanced gestationM Kabra, R Saxena, D Chinnappan, et al.
Indian Journal of Pediatrics|June 11, 2014
Fanconi-Bickel syndrome - mutation in SLC2A2 geneMohit Kehar, Sunita Bijarnia, Sian Ellard, et al.
International Journal of Laboratory Hematology|September 11, 2007
Case report of HbC/beta(0)-thalassemia from IndiaS Kumar, M Rana, A Handoo, et al.
Human Mutation|January 1, 1995
Analysis of beta-thalassemia mutations in the United Arab Emirates provides evidence for recurrent origin of the IVSI nt 5 (G-C) mutationR De Leo, G Deidda, A Novelletto, et al.
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