β-Glucuronidase deficiency as a cause of prenatally diagnosed non-immune hydrops fetalis-Reference-Cited by-同舟云学术

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β-Glucuronidase deficiency as a cause of prenatally diagnosed non-immune hydrops fetalis

Published:1991-06 Issue:6 Volume:11 Page:405-410
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Lissens W.,Dedobbeleer G.,Foulon W.,de Catte L.,Charels K.,Goossens A.,Liebaers I.

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Reference11 articles.

1. Postmortem observations on ?-glucuronidase deficiency presenting as hydrops fetalis

2. Prenatal diagnosis of Hunter syndrome using fetal plasma

3. Differential diagnosis of hydrops fetalis

4. Hydrops revisited: Literature review of 1, 414 cases published in the 1980s

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4. HISTOPATHOLOGICAL DIAGNOSIS OF A TYPE VII MUCOPOLYSACCHARIDOSIS AFTER PREGNANCY TERMINATION;Fetal and Pediatric Pathology;2009-01

5. Mucopolysaccharidosis Type VII (Sly Disease): Clinical, Genetic Diagnosis and Therapies;Lysosomal Storage Disorders;2007

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