Carrier detection and prenatal diagnosis in Norrie disease
D Curtis1, C E Blank, M A Parsons
1Sub-department of Medical Genetics, University of Sheffield, U.K.
Prenatal Diagnosis
|October 1, 1989
Abstract:
We report the use of DNA probes to determine carrier status in three young women from a large kindred with Norrie disease. One of the women requested prenatal diagnosis during pregnancy. In this pedigree, Norrie disease was not characterized by a deletion at DXS7.
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