Items where Author is "Sharif, Fadel A."
Group by: Item Type | No Grouping
Jump to: Article
Number of items: 1.
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