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A novel compound heterozygous HAX1 mutation in a Chinese patient with severe congenital neutropenia and chronic myelomonocytic leukemia transformation but without neurodevelopmental abnormalities
oleh: Sheng-Li Xue, Jin-Li Li, Jing-Ying Zou, Jian Su, Su-Ning Chen, De-Pei Wu
Format: | Article |
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Diterbitkan: | Ferrata Storti Foundation 2012-02-01 |
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