Tay-Sachs Disease: Prenatal Diagnosis-Reference-Cited by-同舟云学术

Tay-Sachs Disease: Prenatal Diagnosis

Published:1971-04-02 Issue:3978 Volume:172 Page:61-64
ISSN:0036-8075
Container-title:Science
language:en
Short-container-title:Science

Author:

O'Brien John S.¹,Okada Shintaro¹,Fillerup Dorothy L.¹,Veath M. Lois¹,Adornato Bruce¹,Brenner Paul H.¹,Leroy Jules G.¹

Affiliation:

1. Departments of Neurosciences and Obstetrics and Gynecology, and University Hospital, School of Medicine, University of California at San Diego, La Jolla 92037

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference13 articles.

1. ARONSON, S.M., TAY SACHS DIS: 118 (1964).

2. KOLODNY, E.H., DEMONSTRATION OF AN ALTERATION OF GANGLIOSIDE METABOLISM IN TAY-SACHS DISEASE, BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 37: 526 (1969).

3. PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENT

4. MACBRINN, M, BETA-GALACTOSIDASE DEFICIENCY IN HURLER SYNDROME, NEW ENGLAND JOURNAL OF MEDICINE 281: 338 (1969).

5. OBRIEN, J.S., GENERALIZED GANGLIOSIDOSIS - ANOTHER INBORN ERROR OF GANGLIOSIDE METABOLISM, AMERICAN JOURNAL OF DISEASES OF CHILDREN 109: 338 (1965).

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