Items where Author is "Sharif, Fadel A."

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Article

Sharif, Fadel A. (2020) An Autosomal Recessive form of Cornelia de Lange Syndrome Due to Mutations in TRMT61A Gene: A Case Report. Journal of Advances in Medicine and Medical Research, 32 (24). pp. 327-331. ISSN 2456-8899

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