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Title: Terminal deletion of the long arm of chromosome 10 : q26 to qter. Case report and review of literature. Author: Taysi K, Strauss AW, Yang V, Padmalatha C, Marshall RE. Journal: Ann Genet; 1982; 25(3):141-4. PubMed ID: 6982660. Abstract: This communication describes the fourth known patient with a terminal long arm deletion of chromosome 10. The karyotype is : 46,XX,del(10)(q26). The clinical findings in the patient included intrauterine growth retardation, microcephaly, truncus arteriosus type 1, respiratory distress and craniofacial dysmorphism. Although review of the limited number of patients with a similar deletion reveals several common features, there is yet insufficient evidence to define a distinct 10q--syndrome.[Abstract] [Full Text] [Related] [New Search]