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Novel and recurrent mutations in WISP3 and an atypical phenotype.
Bhavani GS, Shah H, Dalal AB, Shukla A, Danda S, Aggarwal S, Phadke SR, Gupta N, Kabra M, Gowrishankar K, Gupta A, Bhat M, Puri RD, Bijarnia-Mahay S, Nampoothiri S, Mohanasundaram KM, Rajeswari S, Kulkarni AM, Kulkarni ML, Ranganath P, Ramadevi AR, Hariharan SV, Girisha KM. Bhavani GS, et al. Among authors: phadke sr. Am J Med Genet A. 2015 Oct;167A(10):2481-4. doi: 10.1002/ajmg.a.37164. Epub 2015 May 18. Am J Med Genet A. 2015. PMID: 25988854 No abstract available.
Mseleni and Handigodu familial osteoarthropathies: syndromic identity?
Agarwal SS, Phadke SR, Fredlund V, Viljoen D, Beighton P. Agarwal SS, et al. Among authors: phadke sr. Am J Med Genet. 1997 Nov 12;72(4):435-9. doi: 10.1002/(sici)1096-8628(19971112)72:4<435::aid-ajmg12>3.0.co;2-s. Am J Med Genet. 1997. PMID: 9375727 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