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Page 1
Clinical and mutation profile of multicentric osteolysis nodulosis and arthropathy.
Bhavani GS, Shah H, Shukla A, Gupta N, Gowrishankar K, Rao AP, Kabra M, Agarwal M, Ranganath P, Ekbote AV, Phadke SR, Kamath A, Dalal A, Girisha KM. Bhavani GS, et al. Among authors: dalal a. Am J Med Genet A. 2016 Feb;170A(2):410-417. doi: 10.1002/ajmg.a.37447. Epub 2015 Nov 24. Am J Med Genet A. 2016. PMID: 26601801
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
743 results