Mass screening newborns for mucopolysaccharidoses-Reference-Cited by-同舟云学术

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Mass screening newborns for mucopolysaccharidoses

Published:2008-04-23 Issue:3 Volume:4 Page:260-263
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Sabater J.,Villalba M.,Maya A.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1973.tb01152.x/fullpdf

Reference10 articles.

1. A paper spot test useful in study of Hurler's syndrome;Berry;J. Lab. clin. Med.,1950

2. La pseudo polydystrophie de Hurler;Maroteaux;Presse méd.,1966

3. Le probléme biologique des mucopolysaccharidoses;Maroteaux;Ann. Biol. clin.,1970

4. The genetic mucopolysaccharidoses;McKusick;Medicine (Baltimore),1965

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Neonatal screening for mucopolysaccharidoses by determination of glycosaminoglycans in the eluate of urine-impregnated paper: preliminary results of an improved DMB-based procedure;Journal of Clinical Laboratory Analysis;2010

2. Urinary Glycosaminoglycan Excretion Quantified by an Automated Semimicro Method in Specimens Conveniently Transported from Around the Globe;Molecular Genetics and Metabolism;2002-01

3. Newborn Screening Metabolic Disorders;Clinics in Perinatology;1976-03

4. Chemical and Biochemical Aspects of the Glycosaminoglycans and Proteoglycans in Health and Disease;Advances in Clinical Chemistry Volume 18;1976

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