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Familial Cancer|September 2, 2004
Impact of a cancer registry-based genealogy service to support clinical genetics servicesDavid H Brewster, Alison Fordyce, Roger J Black, et al.
Familial Cancer|June 14, 2005
Ratio of male to female births in the offspring of BRCA1 and BRCA2 carriersG Chenevix-Trench, O M Sinilnikova, G Suthers, et al.
Familial Cancer|August 6, 2008
Genetic testing for BRCA1: effects of a randomised study of knowledge provision on interest in testing and long term test uptake; implications for the NICE guidelinesJulia Hall, Susan Gray, Roger A'Hern, et al.
Familial Cancer|September 17, 2008
Identification and characterization of a novel MLH1 genomic rearrangement as the cause of HNPCC in a Tunisian family: evidence for a homologous Alu-mediated recombinationSana Aissi-Ben Moussa, Amel Moussa, Tonio Lovecchio, et al.
Familial Cancer|October 16, 2008
Prevalence and characteristics of pancreatic cancer in families with BRCA1 and BRCA2 mutationsDaniel H Kim, Beth Crawford, John Ziegler, et al.
Familial Cancer|June 14, 2017
Potentially pathogenic germline CHEK2 c.319+2T>A among multiple early-onset cancer familiesMev Dominguez-Valentin, Sigve Nakken, Hélène Tubeuf, et al.
Familial Cancer|June 16, 2017
Somatic mutations of the coding microsatellites within the beta-2-microglobulin gene in mismatch repair-deficient colorectal cancers and adenomasMark Clendenning, Alvin Huang, Harindra Jayasekara, et al.
Familial Cancer|July 19, 2018
Modified capture-recapture estimates of the number of families with Lynch syndrome in Central OhioJohn Michael O Ranola, Rachel Pearlman, Heather Hampel, et al.
Familial Cancer|May 29, 2017
Quality of life following prophylactic gynecological surgery: experiences of female Lynch mutation carriersHolly Etchegary, Elizabeth Dicks, Laura Tamutis, et al.
Familial Cancer|May 31, 2017
Contiguous gene deletion of chromosome 2p16.3-p21 as a cause of Lynch syndromeErin E Salo-Mullen, Patricio B Lynn, Lu Wang, et al.
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