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Genetic analysis of consanguineous families presenting with congenital ocular defects.
Ullah E, Nadeem Saqib MA, Sajid S, Shah N, Zubair M, Khan MA, Ahmed I, Ali G, Dutta AK, Danda S, Lao R, Ling-Fung Tang P, Kwok PY, Ansar M, Slavotinek A. Ullah E, et al. Among authors: danda s. Exp Eye Res. 2016 May;146:163-171. doi: 10.1016/j.exer.2016.03.014. Epub 2016 Mar 16. Exp Eye Res. 2016. PMID: 26995144
Restrictive Dermopathy.
Dutta AK, Danda S. Dutta AK, et al. Among authors: danda s. Pediatr Neonatol. 2016 Jun;57(3):259. doi: 10.1016/j.pedneo.2015.09.005. Epub 2015 Oct 28. Pediatr Neonatol. 2016. PMID: 26627141 Free article. No abstract available.
Ectodysplasin pathogenic variants affecting the furin-cleavage site and unusual clinical features define X-linked hypohidrotic ectodermal dysplasia in India.
Chaudhary AK, Gholse A, Nagarajaram HA, Dalal AB, Gupta N, Dutta AK, Danda S, Gupta R, Sankar HV, Bhavani GS, Girisha KM, Phadke SR, Ranganath P, Bashyam MD. Chaudhary AK, et al. Among authors: danda s. Am J Med Genet A. 2022 Mar;188(3):788-805. doi: 10.1002/ajmg.a.62579. Epub 2021 Dec 4. Am J Med Genet A. 2022. PMID: 34863015
Founder effects of the homogentisate 1,2-dioxygenase (HGD) gene in a gypsy population and mutation spectrum in the gene among alkaptonuria patients from India.
Danda S, Mohan S, Devaraj P, Dutta AK, Nampoothiri S, Yesodharan D, Phadke SR, Jalan AB, Thangaraj K, Verma IC, Danda D, Jebaraj I. Danda S, et al. Among authors: danda d. Clin Rheumatol. 2020 Sep;39(9):2743-2749. doi: 10.1007/s10067-020-05020-8. Epub 2020 Mar 24. Clin Rheumatol. 2020. PMID: 32212000
156 results