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Identification and characterization of 30 novel pathogenic variations in 69 unrelated Indian patients with Mucolipidosis Type II and Type III.
Pasumarthi D, Gupta N, Sheth J, Jain SJMN, Rungsung I, Kabra M, Ranganath P, Aggarwal S, Phadke SR, Girisha KM, Shukla A, Datar C, Verma IC, Puri RD, Bhavsar R, Mistry M, Sankar VH, Gowrishankar K, Agrawal D, Nair M, Danda S, Soni JP, Dalal A. Pasumarthi D, et al. Among authors: gupta n. J Hum Genet. 2020 Nov;65(11):971-984. doi: 10.1038/s10038-020-0797-8. Epub 2020 Jul 10. J Hum Genet. 2020. PMID: 32651481
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.
8,261 results