Prenatal diagnosis of the Hunter syndrome and the introduction of a new fluorimetric enzyme assay-Reference-Cited by-同舟云学术

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Prenatal diagnosis of the Hunter syndrome and the introduction of a new fluorimetric enzyme assay

Published:2002 Issue:11 Volume:22 Page:1016-1021
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Keulemans J. L. M.,Sinigerska I.,Garritsen V. H.,Huijmans J. G. M.,Voznyi Y. V.,van Diggelen O. P.,Kleijer W. J.

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference19 articles.

1. Prenatal diagnosis of hunter syndrome

2. Full expression of Hunter's disease in a female with an X-chromosome deletion leading to non-random inactivation

3. First-trimester diagnosis of hunter syndrome: Very low iduronate sulphatase activity in chorionic villi from a heterozygous female fetus

4. Intrauterine Diagnosis of the Hurler and Hunter Syndromes

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4. Mucopolysaccharidosis type II (Hunter syndrome): Clinical and biochemical aspects of the disease and approaches to its diagnosis and treatment;Advances in Carbohydrate Chemistry and Biochemistry;2020

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