Human Phosphoglycerate Kinase and Inactivation of the X Chromosome
Author:
Affiliation:
1. Department of Genetics, Division of Biological Sciences; Department of Medicine, Albert Einstein College of Medicine, Bronx, New York 10461
Publisher
American Association for the Advancement of Science (AAAS)
Subject
Multidisciplinary
Reference22 articles.
1. CHEN, S.H., PHOSPHOGLYCERATE KINASE - X-LINKED POLYMORPHISM IN MAN, AMERICAN JOURNAL OF HUMAN GENETICS 23: 87 (1971).
2. COOPER, D.W., DIRECTED GENETIC CHANGE MODEL FOR X CHROMOSOME INACTIVATION IN EUTHERIAN MAMMALS, NATURE 230: 292 (1971).
3. COOPER, D. W., NATURE-NEW BIOLOGY 230: 155 (1971).
4. DANES, B.S., HURLERS SYNDROME - A GENETIC STUDY OF CLONES IN CELL CULTURE WITH PARTICULAR REFERENCE TO LYON HYPOTHESIS, JOURNAL OF EXPERIMENTAL MEDICINE 126: 509 (1967).
5. DAVIDSON, R.G., DEMONSTRATION OF 2 POPULATIONS OF CELLS IN HUMAN FEMALE HETEROZYGOUS FOR GLUCOSE-6-PHOSPHATEDEHYDROGENASE VARIANTS, PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 50: 481 (1963).
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