Difference between revisions of "Myeloid Neoplasms with Germline Predisposition"

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==WHO Classification Pages (Includes Links to Content)==
 
==WHO Classification Pages (Includes Links to Content)==
  
Put your text here, EXAMPLE #[[Chromophobe renal cell carcinoma]]
+
#[[Myeloid Neoplasms with Germline CEBPA Mutation]]
 +
#[[Myeloid Neoplasms with Germline DDX41 Mutation]]
 +
#[[Myeloid Neoplasms with Germline RUNX1 Mutation]]
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#[[Myeloid Neoplasms with Germline ANKRD26 Mutation]]
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#[[Myeloid Neoplasms with Germline ETV6 Mutation]]
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#[[Myeloid Neoplasms with Germline GATA2 Mutation]]
  
 
==Other Related Pages (Includes Links to Content)==
 
==Other Related Pages (Includes Links to Content)==

Revision as of 20:46, 8 June 2019

Primary Author(s)*

Put your text here

General Disease Overview / Description of Cancer Category

Put your text here

WHO Classification Pages (Includes Links to Content)

  1. Myeloid Neoplasms with Germline CEBPA Mutation
  2. Myeloid Neoplasms with Germline DDX41 Mutation
  3. Myeloid Neoplasms with Germline RUNX1 Mutation
  4. Myeloid Neoplasms with Germline ANKRD26 Mutation
  5. Myeloid Neoplasms with Germline ETV6 Mutation
  6. Myeloid Neoplasms with Germline GATA2 Mutation

Other Related Pages (Includes Links to Content)

Put your text here, EXAMPLE #Acute Myeloid Leukemia (AML) with Mutated FLT3

Additional Information

Put your text here

References

EXAMPLE Book

  1. Arber DA, et al., (2008). Acute myeloid leukaemia with recurrent genetic abnormalities, in World Health Organization Classification of Tumours of Haematopoietic and Lymphoid Tissues, 4th edition. Swerdlow SH, Campo E, Harris NL, Jaffe ES, Pileri SA, Stein H, Thiele J, Vardiman JW, Editors. IARC Press: Lyon, France, p117-118.

EXAMPLE Journal Article

  1. Li Y, et al., (2001). Fusion of two novel genes, RBM15 and MKL1, in the t(1;22)(p13;q13) of acute megakaryoblastic leukemia. Nat Genet 28:220-221, PMID 11431691.

Notes

*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.