Prenatal monitoring for the Hunter syndrome: The heterozygous female fetus-Reference-Cited by-同舟云学术

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Prenatal monitoring for the Hunter syndrome: The heterozygous female fetus

Published:2008-04-23 Issue:2 Volume:15 Page:113-117
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

KLEIJER W. J.,MOOY P. D.,LIEBAERS I.,KAMP J. J. P. VAN DE,NIERMEIJER M. F.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1979.tb01749.x/fullpdf

Reference17 articles.

1. The defect in the Hunter syndrome: Deficiency of sulfoiduronate sul-fatase;Bach;Proc. nat. Acad. Sci. (Wash),1973

2. Mosaicism for sulfoiduronate sulfatase deficiency in carriers of Hunter's syndrome;Capobianchi;Ex-perientia,1976

3. Urinary excretion of di-sulfated disaccharides in Hunter syndrome: Correction by infusion of a serum fraction;Coppa;Anal. Lett.,1973

4. Hunter's syndrome: A genetic study of clones in cell culture with particular reference to the Lyon hypothesis;Danes;J. exp. Med.,1967

5. Genetic counseling for Hunter syndrome;Epstein;Lancet,1976

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