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article, google, scholar, cas, dnmta, mutations, leukemia, nature, myelodysplastic, dna, access, patients, syndromes, myeloid, supplementary, mds, cancer, walter, methylation, methyltransferase, content, information, ley, graubert, novo, acute, mutation, essential, cookies, data, aml, domain, cell, syndrome, gene, tet, privacy, ding, dipersio, wilson, study, open, author, research, washington, university, louis, usa, shen, mardis,

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nature portfolio permissions reprints privacy policy mo performed research cancer research advertising nature 1999 nature 2004 nature 2010 nature social media array-based genomic resequencing polycomb-group gene enhancer mammalian development springerlink instant access tg analyzed data idh-mutant astrocytoma progression permissions development 1998 de novo methylation author correspondence dnmt3a mutation status personal data amino acid r882 aberrant dna methylation dna methyltransferase gene recurrent dnmt3a mutations immunodeficiency syndrome caused privacy murine dnmt3a dna dna methyltransferases dnmt3a data protection issue learn generated data acute myeloid leukemia common mutation site supplementary figure 1b dnmt3a-destabilizing variants randomized controlled trial de novo mds explore content subscription content germline atrx mutations european economic area predicted translational consequences local taxes institutional subscriptions read barry-holson kq hidalgo-curtis ce severe hematologic phenotype

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• Common 4q24 deletion in four cases of hematopoietic malignancy: early stem cell involvement?
• Myelodysplastic syndromes: lost between two states?

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