Prenatal diagnosis of Hurler's syndrome?Biochemical studies on the affected fetus-Reference-Cited by-同舟云学术

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Prenatal diagnosis of Hurler's syndrome?Biochemical studies on the affected fetus

Published:1981 Issue:4 Volume:59 Page:353-359
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Ikeno Tomoyasu,Minami Ryoji,Wagatsuma Koji,Fujibayashi Shinsuke,Nakao Tooru,Abo Katsuyuki,Tsugawa Satoshi,Taniguchi Shigeru,Takasago Yuhei

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00295471.pdf

Reference31 articles.

1. Boas NF (1953) Method for the determinations of hexosamines in tissues. J Biol Chem 204:553?563

2. Brock DJH, Gordon H, Seligman S, Lobo EH (1971) Antenatal detection of Hurler syndrome. Lancet 2:1324?1325

3. Brown AH (1946) Determination of pentose in the presence of large quantities of glucose. Arch Biochem Biophys 11:269?278

4. Constantopoulos G, McComb RD, Dekaban AS (1976) Neurochemistry of the mucopolysaccharidoses: Brain glycosaminoglycans in normals and four types of mucopolysaccharidoses. J Neurochem 26: 901?908

5. Constantopoulos G, Dekaban AS (1978) Neurochemistry of the mucopolysaccharidoses: Brain and lysosomal enzymes in patients with four types of mucopolysaccharidosis and in normal controls. J Neurochem 30:965?973

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5. Mucopolysaccharidosis I (MPS I);Atlas of Genetic Diagnosis and Counseling;2012

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