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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: phadke sr. 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
Pachygyria/hypogenitalism: A monogenic syndrome.
Pradhan M, Phadke SR, Jain S, Agarwal SS. Pradhan M, et al. Among authors: phadke sr. Am J Med Genet. 1999 Nov 26;87(3):254-7. Am J Med Genet. 1999. PMID: 10564880 Review.
Neuroimaging in mental retardation.
Pandey A, Phadke SR, Gupta N, Phadke RV. Pandey A, et al. Among authors: phadke rv, phadke sr. Indian J Pediatr. 2004 Mar;71(3):203-9. doi: 10.1007/BF02724269. Indian J Pediatr. 2004. PMID: 15080405
Genetic counseling: the impact in Indian milieu.
Phadke SR, Pandey A, Puri RD, Patil SJ. Phadke SR, et al. Indian J Pediatr. 2004 Dec;71(12):1079-82. doi: 10.1007/BF02829818. Indian J Pediatr. 2004. PMID: 15630315
305 results