Difference between revisions of "GTS5:Volunteer Assignments and Opportunities"

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|[[Constitutional Mismatch Repair Deficiency (CMMRD) Syndrome (MLH1, PMS2, MSH2, MSH6)]]||Disease||Jennie Thurston
+
|[[Neurofibromatosis Type 1 (NF1)]]
|7/2/2023
+
|Disease
 +
|Ngoni Faya (trainee) + Madina Sukhanova
 +
|7/12/2023
 
|
 
|
 
|PENDING
 
|PENDING
 
|
 
|
|LS
+
|Madina Sukhanova (Madina S)
 
|
 
|
 
|Named based on GTS5 book
 
|Named based on GTS5 book
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|Named based on GTS5 book
 
|Named based on GTS5 book
 
|-
 
|-
|[[Neurofibromatosis Type 1 (NF1)]]
+
|[[Constitutional Mismatch Repair Deficiency (CMMRD) Syndrome (MLH1, PMS2, MSH2, MSH6)]]||Disease||Jennie Thurston
|Disease
+
|7/2/2023
|Ngoni Faya (trainee) + Madina Sukhanova
 
|7/12/2023
 
 
|
 
|
 
|PENDING
 
|PENDING
 
|
 
|
|Madina Sukhanova (Madina S)
+
|LS
 
|
 
|
 
|Named based on GTS5 book
 
|Named based on GTS5 book

Revision as of 13:40, 30 December 2023

Welcome!

For assignments, please see the "Author" column below (highlighted blue).

If empty (no name is present), please volunteer to create content for that disease!

To volunteer, please [Contact us] with your page of interest.


WHO Classification of Genetic Tumour Syndromes (5th Edition) Content
Disease Page Type Author Date Assigned to Author Target Completion Date Author Content (Pending or Complete) Date Completed by Author Associate Editor Date of Last Editor Review Notes
CHAPTER 2 (GROWTH FACTOF RECEPTORS AND RELATED SIGNALLING PATHWAYS)

















Neurofibromatosis Type 1 (NF1) Disease Ngoni Faya (trainee) + Madina Sukhanova 7/12/2023 PENDING Madina Sukhanova (Madina S) Named based on GTS5 book
DICER1-Related Tumour Predisposition Syndrome (DICER1) Disease Jennie Thurston 7/2/2023 PENDING LS Named based on GTS5 book
Constitutional Mismatch Repair Deficiency (CMMRD) Syndrome (MLH1, PMS2, MSH2, MSH6) Disease Jennie Thurston 7/2/2023 PENDING LS Named based on GTS5 book
Familial Adenomatous Polyposis (APC) Disease Jennifer Laffin 8/20/2023 PENDING MS / LS Named based on GTS5 book