Identification and characterization of a novel MLH1 genomic rearrangement as the cause of HNPCC in a Tunisian family: evidence for a homologous Alu-mediated recombination-Reference-Cited by-同舟云学术

Identification and characterization of a novel MLH1 genomic rearrangement as the cause of HNPCC in a Tunisian family: evidence for a homologous Alu-mediated recombination

Published:2008-09-16 Issue:2 Volume:8 Page:119-126
ISSN:1389-9600
Container-title:Familial Cancer
language:en
Short-container-title:Familial Cancer

Author:

Aissi-Ben Moussa Sana,Moussa Amel,Lovecchio Tonio,Kourda Nadia,Najjar Taoufik,Ben Jilani Sarra,El Gaaied Amel,Porchet Nicole,Manai Mohamed,Buisine Marie-Pierre

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Genetics (clinical),Oncology,Genetics

Link

http://link.springer.com/content/pdf/10.1007/s10689-008-9215-7.pdf

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3. Olschwang S, Bonaïti-Pellié C, Feingold J et al (2006) Identification and management of HNPCC syndrome (hereditary non polyposis colon cancer), hereditary predisposition to colorectal and endometrial adenocarcinomas. Pathol Biol 54:215–229. doi: 10.1016/j.patbio.2006.02.008

4. Hendriks YM, Jagmohan-Changur S, van der Klift HM et al (2006) Heterozygous mutations in PMS2 cause hereditary nonpolyposis colorectal carcinoma (Lynch syndrome). Gastroenterology 130:312–322. doi: 10.1053/j.gastro.2005.10.052

5. Lagerstedt-Robinson K, Liu T, Vandrovcova J, Halvarsson B et al (2007) Lynch syndrome (hereditary nonpolyposis colorectal cancer) diagnostics. J Natl Cancer Inst 99:291–299. doi: 10.1093/jnci/djk051

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