Volume 10, Issue 4

December 2011

“The Proceedings of the Collaborative Group of the Americas on Inherited Colorectal Cancer” Delta Centre-Ville Hotel, Montreal, Quebec, Canada, October 10-11, 2011

14 articles in this issue

Familial colorectal cancer type X syndrome: two distinct molecular entities?
Inês Francisco
Cristina Albuquerque
António Dias Pereira
OriginalPaper 12 August 2011 Pages: 623 - 631
Limited impact on self-concept in individuals with Lynch syndrome; results from a national cohort study
Helle Vendel Petersen
Mary Jane Esplen
Mef Nilbert
OriginalPaper 21 June 2011 Pages: 633 - 639
Characterization of germline mutations of MLH1 and MSH2 in unrelated south American suspected Lynch syndrome individuals
Mev Dominguez Valentin
Felipe Carneiro da Silva
Benedito Mauro Rossi
OriginalPaper 17 June 2011 Pages: 641 - 647
Factors affecting encouragement of relatives among families with Lynch syndrome to seek medical assessment
Noriko Ishii
Masami Arai
Tetsuichiro Muto
OriginalPaper 22 June 2011 Pages: 649 - 654
Microsatellite instability analysis in uterine cavity washings as a screening tool for endometrial cancer in Lynch syndrome
Julie Bouquier
Hélène Blons
Anne-Sophie Bats
BriefCommunication 06 August 2011 Pages: 655 - 657
A survey of APC mutations in Quebec
Jonathan Jarry
Jean-Sébastien Brunet
George Chong
OriginalPaper 22 July 2011 Pages: 659 - 665
The identification and management of hereditary diffuse gastric cancer in a large Jordanian family
Henry T. Lynch
Ibrahim Aldoss
Jane F. Lynch
OriginalPaper 17 June 2011 Pages: 667 - 672
Communication of BRCA1 and BRCA2 genetic test results to health care providers following genetic testing at a tertiary care center
K. Ready
B. K. Arun
S. K. Peterson
OriginalPaper 17 June 2011 Pages: 673 - 679
Concerns about inherited risk of breast cancer prior to diagnosis in Japanese patients with breast complaints
Noriko Ando
Yumi Iwamitsu
Hitoshi Miyaoka
OriginalPaper 24 June 2011 Pages: 681 - 689
Acinic cell carcinoma of the retromolar trigone region: expanding the tumor phenotype in Cowden syndrome?
Hugo Villeneuve
Steve Tremblay
Marc Tischkowitz
BriefCommunication 06 August 2011 Pages: 691 - 694
Novel nonsense CDC73 mutations in Chinese patients with parathyroid tumors
Wai Kwan Siu
Chun Yiu Law
Albert Yan Wo Chan
OriginalPaper 06 July 2011 Pages: 695 - 699
Long-term outcomes, branch-specific expressivity, and disease-related mortality in von Hippel-Lindau type 2A
Sarah M. Nielsen
Wendy S. Rubinstein
Sally E. Carty
OriginalPaper 29 June 2011 Pages: 701 - 707
Identification of the deleterious 2080insA BRCA1 mutation in a male renal cell carcinoma patient from a family with multiple cancer diagnoses from Pakistan
Muhammad U. Rashid
Sidra Gull
Ute Hamann
Letter to the Editor 13 July 2011 Pages: 709 - 712
Abstracts

Abstract 13 December 2011 Pages: 713 - 743

Volume 10, Issue 4

Familial colorectal cancer type X syndrome: two distinct molecular entities?

Limited impact on self-concept in individuals with Lynch syndrome; results from a national cohort study

Characterization of germline mutations of MLH1 and MSH2 in unrelated south American suspected Lynch syndrome individuals

Factors affecting encouragement of relatives among families with Lynch syndrome to seek medical assessment

Microsatellite instability analysis in uterine cavity washings as a screening tool for endometrial cancer in Lynch syndrome

A survey of APC mutations in Quebec

The identification and management of hereditary diffuse gastric cancer in a large Jordanian family

Communication of BRCA1 and BRCA2 genetic test results to health care providers following genetic testing at a tertiary care center

Concerns about inherited risk of breast cancer prior to diagnosis in Japanese patients with breast complaints

Acinic cell carcinoma of the retromolar trigone region: expanding the tumor phenotype in Cowden syndrome?

Novel nonsense CDC73 mutations in Chinese patients with parathyroid tumors

Long-term outcomes, branch-specific expressivity, and disease-related mortality in von Hippel-Lindau type 2A

Identification of the deleterious 2080insA BRCA1 mutation in a male renal cell carcinoma patient from a family with multiple cancer diagnoses from Pakistan

Abstracts

Navigation

Volume 10, Issue 4

Search

Navigation