LYONISATION OF THE X CHROMOSOME
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference8 articles.
1. X-CHROMOSOME MOSAICISM IN FEMALES WITH MUSCULAR DYSTROPHY
2. CLINICAL MANIFESTATIONS IN TWO CARRIERS OF DUCHENNE MUSCULAR DYSTROPHY
3. Electrophoretic Pattern of Lactic Dehydrogenase in Carriers and Patients with Duchenne Muscular Dystrophy
4. DNA synthesis and myogenesis
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1. STUDIES ON HUMAN MUSCULAR DYSTROPHY WITH PARTICULAR REFERENCE TO METHODS OF CARRIER DETECTION;Annals of the New York Academy of Sciences;2006-12-16
2. THE VALUE OF SERUM ENZYME DETERMINATIONS IN THE IDENTIFICATION OF DYSTROPHIC CARRIERS;Annals of the New York Academy of Sciences;2006-12-16
3. Duchenne muscular dystrophy: Pathogenetic aspects and genetic prevention;Human Genetics;1984-03
4. THE USE OF EARLY EMBRYO AGGREGATION DERIVED MOUSE CHIMAERAS. II. THE STUDY OF DISEASE PROCESSES;European Journal of Immunogenetics;1976-12
5. Chimaera mouse study shows absence of disease in genetically dystrophic muscle;Nature;1974-04
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