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Title: Severe midline fusion defects in a newborn with 10q26----qter deletion. Author: Fryns JP, Kleczkowska A, Fivez H, Van den Berghe H. Journal: Ann Genet; 1989; 32(2):124-5. PubMed ID: 2757362. Abstract: In this report we describe a male newborn with a severe midline fusion syndrome associated with a "pure" distal 10q deletion (del(10)(q26.1----qter].[Abstract] [Full Text] [Related] [New Search]