Volume 12, Issue 1

Search all Familial Cancer articles

March 2013

18 articles in this issue

10 rare tumors that warrant a genetics referral
Kimberly C. Banks
Jessica J. Moline
Kristen J. Vogel
Review 28 November 2012 Pages: 1 - 18
Catalysts to withdrawal from familial ovarian cancer screening for surgery and reactions to discontinued screening: a qualitative study
Kate J. Lifford
Alison Clements
Kate Brain
Original Article 27 September 2012 Pages: 19 - 26
Somatic mosaicism and double somatic hits can lead to MSI colorectal tumors
Isabelle Sourrouille
Florence Coulet
Florent Soubrier
Original Article 18 September 2012 Pages: 27 - 33
Novel mutations of the APC gene and genetic consequences of splicing mutations in the Czech FAP families
Lucie Schwarzová
Jitka Štekrová
Milada Kohoutová
Original Article 18 September 2012 Pages: 35 - 42
Contribution of bi-allelic germline MUTYH mutations to early-onset and familial colorectal cancer and to low number of adenomatous polyps: case-series and literature review
A. P. Knopperts
M. Nielsen
F. J. Hes
Original Article 25 September 2012 Pages: 43 - 50
Prospective enteroscopic evaluation of jejunal polyposis in patients with familial adenomatous polyposis and advanced duodenal polyposis
Y. A. Alderlieste
E. A. J. Rauws
E. Dekker
Original Article 29 September 2012 Pages: 51 - 56
The spectrum of urological malignancy in Lynch syndrome
P. J. Barrow
S. Ingham
D. G. Evans
Original Article 11 October 2012 Pages: 57 - 63
Feasibility evaluation of an online tool to guide decisions for BRCA1/2 mutation carriers
Elizabeth A. Schackmann
Diego F. Munoz
Allison W. Kurian
Original Article 21 October 2012 Pages: 65 - 73
The prevalence of BRCA mutations among familial breast cancer patients in Korea: results of the Korean Hereditary Breast Cancer study
Sang-Ah Han
Sung-Won Kim
The KOHBRA Research Group and the Korean Breast Cancer Society
Original Article 07 November 2012 Pages: 75 - 81
An unusual BRCA mutation distribution in a high risk cancer genetics clinic
Anna C. Nelson-Moseke
Joanne M. Jeter
Christina M. Laukaitis
Original Article 21 November 2012 Pages: 83 - 87
Multiple small “imaging” branch-duct type intraductal papillary mucinous neoplasms (IPMNs) in familial pancreatic cancer: indicator for concomitant high grade pancreatic intraepithelial neoplasia?
D. K. Bartsch
K. Dietzel
P. Langer
Original Article 22 November 2012 Pages: 89 - 96
Birt–Hogg–Dubé: beyond the clinical manifestations
Lindsay A. Middelton
Original Article 23 November 2012 Pages: 97 - 99
Psychosocial factors and uptake of risk-reducing salpingo-oophorectomy in women at high risk for ovarian cancer
Bettina Meiser
Melanie A. Price
Kelly-Anne Phillips
Original Article 01 December 2012 Pages: 101 - 109
A novel missense mutation (N78D) in a family with von Hippel–Lindau disease with central nervous system haemangioblastomas, pancreatic and renal cysts
S. Cingoz
R. B. van der Luijt
Mihriban Heval Ozgen
Original Article 09 December 2012 Pages: 111 - 117
The deletion of exons 3–5 of BRCA1 is the first founder rearrangement identified in breast and/or ovarian cancer Spanish families
Sarai Palanca
Inmaculada de Juan
Pascual Bolufer
Short Communication 02 November 2012 Pages: 119 - 123
Absence of loss of heterozygosity of BRCA1 in a renal tumor from a BRCA1 germline mutation carrier
Shaheen Alanee
Sohela Shah
Kenneth Offit
Letter to the Editor 20 October 2012 Pages: 125 - 127
Value of bilateral breast cancer for identification of rare recessive at-risk alleles: evidence for the role of homozygous GEN1 c.2515_2519delAAGTT mutation
Ekatherina Sh. Kuligina
Anna P. Sokolenko
Evgeny N. Imyanitov
Letter to the Editor 27 October 2012 Pages: 129 - 132
The Fourth Birt–Hogg–Dubé Symposium, Cincinnati, USA, 28^th–30^th March, 2012

Abstracts 03 July 2012 Pages: 133 - 140

Volume 12, Issue 1

10 rare tumors that warrant a genetics referral

Catalysts to withdrawal from familial ovarian cancer screening for surgery and reactions to discontinued screening: a qualitative study

Somatic mosaicism and double somatic hits can lead to MSI colorectal tumors

Novel mutations of the APC gene and genetic consequences of splicing mutations in the Czech FAP families

Contribution of bi-allelic germline MUTYH mutations to early-onset and familial colorectal cancer and to low number of adenomatous polyps: case-series and literature review

Prospective enteroscopic evaluation of jejunal polyposis in patients with familial adenomatous polyposis and advanced duodenal polyposis

The spectrum of urological malignancy in Lynch syndrome

Feasibility evaluation of an online tool to guide decisions for BRCA1/2 mutation carriers

The prevalence of BRCA mutations among familial breast cancer patients in Korea: results of the Korean Hereditary Breast Cancer study

An unusual BRCA mutation distribution in a high risk cancer genetics clinic

Multiple small “imaging” branch-duct type intraductal papillary mucinous neoplasms (IPMNs) in familial pancreatic cancer: indicator for concomitant high grade pancreatic intraepithelial neoplasia?

Birt–Hogg–Dubé: beyond the clinical manifestations

Psychosocial factors and uptake of risk-reducing salpingo-oophorectomy in women at high risk for ovarian cancer

A novel missense mutation (N78D) in a family with von Hippel–Lindau disease with central nervous system haemangioblastomas, pancreatic and renal cysts

The deletion of exons 3–5 of BRCA1 is the first founder rearrangement identified in breast and/or ovarian cancer Spanish families

Absence of loss of heterozygosity of BRCA1 in a renal tumor from a BRCA1 germline mutation carrier

Value of bilateral breast cancer for identification of rare recessive at-risk alleles: evidence for the role of homozygous GEN1 c.2515_2519delAAGTT mutation

The Fourth Birt–Hogg–Dubé Symposium, Cincinnati, USA, 28^th–30^th March, 2012

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