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Subjects
Congresses, Genetic Diseases, Inborn, Genetic disorders, Genetics, Hemoglobinuria, Paroxysmal, Inborn Genetic Diseases, Molecular aspects, Molecular aspects of Myelodysplastic syndromes, Molecular aspects of Paroxysmal hemoglobinuria, Molecular biology, Myelodysplastic syndromes, Paroxysmal hemoglobinuriaID Numbers
- OLID: OL5689242A
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October 21, 2008 | Created by ImportBot | Imported from Library of Congress MARC record |