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Page 1
Recurrent and novel GLB1 mutations in India.
Bidchol AM, Dalal A, Trivedi R, Shukla A, Nampoothiri S, Sankar VH, Danda S, Gupta N, Kabra M, Hebbar SA, Bhat RY, Matta D, Ekbote AV, Puri RD, Phadke SR, Gowrishankar K, Aggarwal S, Ranganath P, Sharda S, Kamate M, Datar CA, Bhat K, Kamath N, Shah H, Krishna S, Gopinath PM, Verma IC, Nagarajaram HA, Satyamoorthy K, Girisha KM. Bidchol AM, et al. Among authors: gupta n. Gene. 2015 Aug 10;567(2):173-81. doi: 10.1016/j.gene.2015.04.078. Epub 2015 Apr 30. Gene. 2015. PMID: 25936995
Neuroimaging in mental retardation.
Pandey A, Phadke SR, Gupta N, Phadke RV. Pandey A, et al. Among authors: gupta n. Indian J Pediatr. 2004 Mar;71(3):203-9. doi: 10.1007/BF02724269. Indian J Pediatr. 2004. PMID: 15080405
Unbalanced X; autosome translocation.
Gupta N, Goel H, Phadke SR. Gupta N, et al. Indian J Pediatr. 2006 Sep;73(9):840-2. doi: 10.1007/BF02790399. Indian J Pediatr. 2006. PMID: 17006048
Maffucci syndrome.
Gupta N, Kabra M. Gupta N, et al. Indian Pediatr. 2007 Feb;44(2):149-50. Indian Pediatr. 2007. PMID: 17351310 Free article. No abstract available.
Pyle metaphyseal dysplasia.
Gupta N, Kabra M, Das CJ, Gupta AK. Gupta N, et al. Among authors: gupta ak. Indian Pediatr. 2008 Apr;45(4):323-5. Indian Pediatr. 2008. PMID: 18451455 Free article.
8,629 results