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Prenatal diagnosis of a large heteromorphic region in a chromosome 5: implications for genetic counseling.

作者信息

Fineman R M, Issa B, Weinblatt V

机构信息

Department of Pediatrics, University of Utah School of Medicine, Salt Lake City 84132.

出版信息

Am J Med Genet. 1989 Apr;32(4):498-9. doi: 10.1002/ajmg.1320320414.

Abstract

We performed an amniotic fluid chromosome study at 16 weeks of gestation because of advanced maternal age. G-band chromosome analysis demonstrated that one 5q was significantly longer than its homologue. The region subjacent to the centromere appeared similar to a 9qh region. Subsequent Giemsa-11 and C-band staining results of this area were positive. Cytogenetic studies in this family demonstrated several other individuals who have the same chromosome 5qh+ as the proposita. All are asymptomatic. The clinical insignificance of the chromosome heteromorphism in this family readily demonstrates the need for special cytogenetic and family chromosome studies before performing genetic counseling.

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