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Subjects
Abnormalities, human, Diagnosis, Genetic disorders, Multiple Abnormalities, Therapy, Inborn Genetic Diseases, Aanleg, Abnormalities, Angelman syndrome, Anomalia craniofacial, Chromosome Abnormalities, Chromosomes, Human, Pair 15, Congresses, Erbkrankheit, Erfelijke ziekten, Genetica, Herediatary Diseases, Human chromosome 15, Maladies hereditaires, Pathology, Prader-Willi Syndrome, Prader-Willi syndrome, Prader-willi syndrome, Sindromes orofaciodigitais, SyndromID Numbers
- OLID: OL7893104A
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May 15, 2020 | Created by ImportBot | import new book |