Fabry's Disease: Antenatal Detection-Reference-Cited by-同舟云学术

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Fabry's Disease: Antenatal Detection

Published:1971-04-09 Issue:3979 Volume:172 Page:174-175
ISSN:0036-8075
Container-title:Science
language:en
Short-container-title:Science

Author:

Brady Roscoe O.¹,Uhlendorf B. William²,Jacobson Cecil B.³

Affiliation:

1. Laboratory of Neurochemistry, National Institute of Neurological Diseases and Blindness, Bethesda, Maryland 20014

2. Division of Biologics Standards, National Institutes of Health, Bethesda, Maryland 20014

3. Department of Obstetrics and Gynecology, George Washington University School of Medicine, Washington, D.C. 20005

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference12 articles.

1. BRADY, R.O., METABOLISM OF CERAMIDE TRIHEXOSIDES .I. PURIFICATION AND PROPERTIES OF AN ENZYME THAT CLEAVES TERMINAL GALACTOSE MOLECULE OF GALACTOSYLGALACTOSYLGLUCOSYLCERAMIDE, JOURNAL OF BIOLOGICAL CHEMISTRY 242: 1021 (1967).

2. BRADY, R.O., ENZYMATIC DEFECT IN FABRYS DISEASE - CERAMIDETRIHEXOSIDASE DEFICIENCY, NEW ENGLAND JOURNAL OF MEDICINE 276: 1163 (1967).

3. COLOWICK, S.P., METHODS ENZYMOL 1: 34 (1955).

4. DUBACH, U.C., GER MED MON 14: 34 (1969).

5. JACOBSON, C.B., INTRAUTERINE DIAGNOSIS AND MANAGEMENT OF GENETIC DEFECTS, AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY 99: 796 (1967).

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