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2. Bellissimo, D.C. and Speck, N. A. (2017). RUNX1 Mutations in Inherited and Sporadic Leukemia. Front Cell Dev. Biol. 5: 111  PMID 29326930  10.3389/fcell.2017.00111
 
2. Bellissimo, D.C. and Speck, N. A. (2017). RUNX1 Mutations in Inherited and Sporadic Leukemia. Front Cell Dev. Biol. 5: 111  PMID 29326930  10.3389/fcell.2017.00111
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3. Wang, > et al. (2017).  Molecular Mutations and Their Cooccurrences in Cytogenetically Normal Acute Myeloid Leukemia.  Stem Cells Int. 2017:6962379  PMID 28197208  doi: 10.1155/2017/6962379
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3. Wang, et al. (2017).  Molecular Mutations and Their Cooccurrences in Cytogenetically Normal Acute Myeloid Leukemia.  Stem Cells Int. 2017:6962379  PMID 28197208  doi: 10.1155/2017/6962379
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4 . Kamikubo, Y. (2018).  Genetic compensation of RUNX family transcription factors in leukemia. Cancer Sci. (online version ahead of publication). PMID 29883054 doi.org/10.1111/cas.13664
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4 . Kamikubo, Y. (2018).  Genetic compensation of RUNX family transcription factors in leukemia. Cancer Sci. (online version ahead of publication). PMID 29883054 doi.org/10.1111/cas.13664.
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5. book
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6. Taylor, J. et al. (2017). Diagnosis and classification of hematologic malignancies on the basis of genetics. Blood. 130:410-423. PMID 28600336  doi: 10.1182/blood-2017-02-734541
    
== Notes ==
 
== Notes ==
 
<nowiki>*</nowiki>Primary authors will typically be those that initially create and complete the content of a page.  If a subsequent user modifies the content and feels the effort put forth is of high enough significance to warrant listing in the authorship section, please contact the CCGA coordinators (contact information provided on the homepage).  Additional global feedback or concerns are also welcome.
 
<nowiki>*</nowiki>Primary authors will typically be those that initially create and complete the content of a page.  If a subsequent user modifies the content and feels the effort put forth is of high enough significance to warrant listing in the authorship section, please contact the CCGA coordinators (contact information provided on the homepage).  Additional global feedback or concerns are also welcome.
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