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The Roberts Syndrome: A Case Report of an Infant with Valvular Aortic Stenosis and Mutation in ESCO2
Dogan, Mustafa; Firinci, Fatih; Balci, Yasemin Isik; Zeybek, Selcan; Ozgurler, Funda; Erdogan, Ilkay; Varan, Birgul; Semerci, Cavidan Nur (2014)Roberts syndrome, which is inherited as an autosomal recessive group of disorders, is a rare syndrome characterized with symmetrical extremity defects, craniofacial abnormalities, and prenatal and postnatal growth retardation. ...