| Literature DB >> 5547732 |
R O Brady, B W Uhlendorf, C B Jacobson.
Abstract
A procedure is described for the intrauterine detection, at the 17th week of gestation, of a male fetus afflicted with Fabry's disease. The validity of this determination was substantiated by multiple enzyme and lipid analyses of tissue specimens obtained from the afflicted fetus. Fabry's disease may now be included with other X-linked metabolic deficiency diseases that are amenable to precise genetic counseling, through carrier identification, and the monitoring of ensuing pregnancies.Entities:
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Year: 1971 PMID： 5547732 DOI： 10.1126/science.172.3979.174
Source DB: PubMed Journal: Science ISSN： 0036-8075 Impact factor: 47.728