𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Reply to “Reassessing the TARBP2 mutation rate in hereditary nonpolyposis colorectal cancer”

✍ Scribed by Melo, Sonia A; Esteller, Manel

Book ID
109918114
Publisher
Nature Publishing Group
Year
2010
Tongue
English
Weight
68 KB
Volume
42
Category
Article
ISSN
1061-4036

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Mutation of the hMSH2 gene in two famili
Mutation of the hMSH2 gene in two families with hereditary nonpolyposis colorectal cancer
✍ Hae Mung Jeon; Patrick M. Lynch; Linda Howard; Jaffer Ajani; Bernard Levin; Mars 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 554 KB

Communicated by Sauiu L.C. Woo We examined 18 unrelated individuals who have colorectal cancer or cancers associated with the HNPCC syndrome and have a family history of cancer for mutations in exon 13 of the hMSH2 gene. Two of the 18 individuals had the same previously unreported single-base delet

MLH1 and MSH2 constitutinal mutations in
MLH1 and MSH2 constitutinal mutations in colorectal cancer families not meeting the standard criteria for hereditary nonpolyposis colorectal cancer
✍ Maurizio Genuardi; Marcello Anti; Eugenia Capozzi; Francesca Leonardi; Mara Forn 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 French ⚖ 67 KB 👁 2 views

## Genetic diagnosis of hereditary nonpolyposis colorectal cancer (HNPCC ) may have a significant impact on the clinical management of patients and their at-risk relatives. At present, clinical criteria represent the simplest and most useful method for the identification of HNPCC families and for