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Spectrum of SMPD1 mutations in Asian-Indian patients with acid sphingomyelinase (ASM)-deficient Niemann-Pick disease.
Ranganath P, Matta D, Bhavani GS, Wangnekar S, Jain JM, Verma IC, Kabra M, Puri RD, Danda S, Gupta N, Girisha KM, Sankar VH, Patil SJ, Ramadevi AR, Bhat M, Gowrishankar K, Mandal K, Aggarwal S, Tamhankar PM, Tilak P, Phadke SR, Dalal A. Ranganath P, et al. Among authors: dalal a. Am J Med Genet A. 2016 Oct;170(10):2719-30. doi: 10.1002/ajmg.a.37817. Epub 2016 Jun 24. Am J Med Genet A. 2016. PMID: 27338287
Hemihyperplasia syndromes.
Dalal AB, Phadke SR, Pradhan M, Sharda S. Dalal AB, et al. Indian J Pediatr. 2006 Jul;73(7):609-15. doi: 10.1007/BF02759927. Indian J Pediatr. 2006. PMID: 16877856
Handless, footless fetus.
Phadke SR, Girisha KM, Dalal A. Phadke SR, et al. Among authors: dalal a. Clin Dysmorphol. 2006 Oct;15(4):233-234. doi: 10.1097/01.mcd.0000220612.63025.4b. Clin Dysmorphol. 2006. PMID: 16957480
Morphometric analysis of face in dysmorphology.
Dalal AB, Phadke SR. Dalal AB, et al. Comput Methods Programs Biomed. 2007 Feb;85(2):165-72. doi: 10.1016/j.cmpb.2006.10.005. Epub 2006 Nov 21. Comput Methods Programs Biomed. 2007. PMID: 17118483
A founder ectodysplasin A receptor (EDAR) mutation results in a high frequency of the autosomal recessive form of hypohidrotic ectodermal dysplasia in India.
Bashyam MD, Chaudhary AK, Reddy EC, Reddy V, Acharya V, Nagarajaram HA, Devi AR, Bashyam L, Dalal AB, Gupta N, Kabra M, Agarwal M, Phadke SR, Tainwala R, Kumar R, Hariharan SV. Bashyam MD, et al. Among authors: dalal ab. Br J Dermatol. 2012 Apr;166(4):819-29. doi: 10.1111/j.1365-2133.2011.10707.x. Epub 2012 Mar 5. Br J Dermatol. 2012. PMID: 22032522
782 results