An unusual form of galactosemia: Studies on erythrocytes and hair roots-Reference-Cited by-同舟云学术

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An unusual form of galactosemia: Studies on erythrocytes and hair roots

Published:2008-06-28 Issue:1 Volume:13 Page:8-16
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Bruyn C. H. M. M.,Oei T. L.,Monnens L. A. H.,Trijbels J. M. F.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1978.tb04124.x/fullpdf

Reference24 articles.

1. Improved method for measuring galactose-1-phosphate uridyl transferase of erythrocytes;Beutler;Clin. chim. Acta,1966

2. The genetics of galactose-1-phosphate uridyl transferase deficiency;Beutler;J. Lab. din. Med.,1966

3. Studies on hair roots for carrier detection in hypoxanthine-guanine phosphoribosyl transferase deficiency;Bruyn;Clin. Genet.,1974

4. Galactose-1-phosphate uridyl transferase activities in erythrocytes from a patient with galactosemia;Bruyn;Clin. chim. Acta.,1977a

Cited by 2 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. Differentiation of hair growth cycle from scalp hair roots for the diagnosis of glucose-6-phosphate dehydrogenase deficiency in neonates;Journal of Inherited Metabolic Disease;2000-11

2. Purification and characterization of human erythrocyte uridylyl transferase;Biochimica et Biophysica Acta (BBA) - Enzymology;1981-02

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