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Familial Cancer|March 9, 2013
Genetic modifiers of cancer risk in Lynch syndrome: a reviewBente A Talseth-Palmer, Juul T Wijnen, Desma M Grice, et al.Familial Cancer|March 9, 2013
The incidence of PALB2 c.3113G>A in women with a strong family history of breast and ovarian cancer attending familial cancer centres in AustraliaZhi L Teo, Sarah D Sawyer, Paul A James, et al.Familial Cancer|February 20, 2013
Role of new endoscopic techniques in Lynch syndromeJasmijn F Haanstra, Jan H Kleibeuker, Jan J KoornstraFamilial Cancer|September 5, 2013
Reflex testing for Lynch syndrome: if we build it, will they come? Lessons learned from the uptake of clinical genetics services by individuals with newly diagnosed colorectal cancer (CRC)E Tomiak, A Samson, N Spector, et al.Familial Cancer|July 23, 2014
Phenotype of SDHB mutation carriers in the NetherlandsLeonie T van Hulsteijn, Nienke D Niemeijer, Frederik J Hes, et al.Familial Cancer|July 26, 2013
The MDM2 285G-309G haplotype is associated with an earlier age of tumour onset in patients with Li-Fraumeni syndromeMariette Renaux-Petel, Richard Sesboüé, Stéphanie Baert-Desurmont, et al.Familial Cancer|August 10, 2014
The secondary bile acid, deoxycholate accelerates intestinal adenoma-adenocarcinoma sequence in Apc (min/+) mice through enhancing Wnt signalingHailong Cao, Shenhui Luo, Mengque Xu, et al.Familial Cancer|December 21, 2011
Hereditary medullary thyroid carcinoma: the management dilemmaPing Zhou, Jian Liu, Shao-Wen Cheng, et al.Familial Cancer|December 22, 2011
Risk of cancer other than breast or ovarian in individuals with BRCA1 and BRCA2 mutationsA Moran, C O'Hara, S Khan, et al.Familial Cancer|December 15, 2012
Cancer family history triage: a key step in the decision to offer screening and genetic testingPaul Brennan, Oonagh Claber, Tracey BrennanPageof 152