Difference between revisions of "GTS5:Volunteer Assignments and Opportunities"
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To volunteer, please '''[[Mailto:CCGA@cancergenomics.org <u>Contact us</u>]]''' with your page of interest. | To volunteer, please '''[[Mailto:CCGA@cancergenomics.org <u>Contact us</u>]]''' with your page of interest. | ||
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{| class="wikitable" style="margin:auto" | {| class="wikitable" style="margin:auto" | ||
|+<big>WHO Classification of Genetic Tumour Syndromes (5th Edition) Content</big> | |+<big>WHO Classification of Genetic Tumour Syndromes (5th Edition) Content</big> | ||
Line 770: | Line 477: | ||
|[[GTS5:Von_Hippel-Lindau_syndrome_(VHL)|Von Hippel-Lindau syndrome (VHL)]] | |[[GTS5:Von_Hippel-Lindau_syndrome_(VHL)|Von Hippel-Lindau syndrome (VHL)]] | ||
|Disease | |Disease | ||
+ | |Lakshmi Chandramohan | ||
+ | |6/24/24 | ||
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+ | |PENDING | ||
| | | | ||
| | | | ||
| | | | ||
− | | | + | |Named based on GTS5 book (page created 6/24/24) |
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|- | |- | ||
|[[GTS5:SDH-deficient_tumour_syndrome_-_Hereditary_phaeochromocytoma-paraganglioma_syndromes_(SDHA,_SDHB,_SDHC,_SDHD,_SDHAF2)|SDH-deficient tumour syndrome - Hereditary phaeochromocytoma-paraganglioma syndromes (SDHA, SDHB, SDHC, SDHD, SDHAF2)]] | |[[GTS5:SDH-deficient_tumour_syndrome_-_Hereditary_phaeochromocytoma-paraganglioma_syndromes_(SDHA,_SDHB,_SDHC,_SDHD,_SDHAF2)|SDH-deficient tumour syndrome - Hereditary phaeochromocytoma-paraganglioma syndromes (SDHA, SDHB, SDHC, SDHD, SDHAF2)]] | ||
Line 834: | Line 541: | ||
|[[GTS5:Li-Fraumeni_syndrome_(TP53)|Li-Fraumeni syndrome (TP53)]] | |[[GTS5:Li-Fraumeni_syndrome_(TP53)|Li-Fraumeni syndrome (TP53)]] | ||
|Disease | |Disease | ||
+ | |Lakshmi Chandramohan | ||
+ | |6/24/24 | ||
| | | | ||
− | | | + | |PENDING |
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Line 986: | Line 693: | ||
|[[GTS5:Fanconi_anaemia_(FANC_genes)|Fanconi anaemia (FANC genes)]] | |[[GTS5:Fanconi_anaemia_(FANC_genes)|Fanconi anaemia (FANC genes)]] | ||
|Disease | |Disease | ||
+ | |Nada Assaf | ||
+ | |6/11/2024 | ||
| | | | ||
+ | |PENDING | ||
| | | | ||
+ | |Eric McGinnis | ||
| | | | ||
− | | | + | |Named based on GTS5 book |
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|- | |- | ||
|[[GTS5:MUTYH-associated_polyposis_(MUTYH)|MUTYH-associated polyposis (MUTYH)]] | |[[GTS5:MUTYH-associated_polyposis_(MUTYH)|MUTYH-associated polyposis (MUTYH)]] | ||
Line 1,085: | Line 792: | ||
|[[GTS5:Bloom_syndrome_(BLM)|Bloom syndrome (BLM)]] | |[[GTS5:Bloom_syndrome_(BLM)|Bloom syndrome (BLM)]] | ||
|Disease | |Disease | ||
+ | |Nada Assaf | ||
+ | |6/11/2024 | ||
| | | | ||
+ | |PENDING | ||
| | | | ||
+ | |Xiaolin (Lynn) Hu | ||
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− | | | + | |Named based on GTS5 book |
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|- | |- | ||
|[[GTS5:Werner_syndrome_(WRN)|Werner syndrome (WRN)]] | |[[GTS5:Werner_syndrome_(WRN)|Werner syndrome (WRN)]] |
Latest revision as of 12:59, 24 June 2024
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.