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Familial Cancer|May 1, 2014
Exploring the association of succinate dehydrogenase complex mutations with lymphoid malignanciesR Renella, J Carnevale, K A Schneider, et al.
Familial Cancer|April 29, 2014
BRCA1 founder mutations compared to ovarian cancer in BelarusAlena Savanevich, Oleg Oszurek, Jan Lubiński, et al.
Familial Cancer|June 12, 2012
Causes of death of mutation carriers in Finnish Lynch syndrome familiesKirsi Pylvänäinen, Tuula Lehtinen, Ilmo Kellokumpu, et al.
Familial Cancer|September 24, 2014
Outcomes of genetic evaluation for hereditary cancer syndromes in unaffected individualsShanna L Gustafson, Victoria M Raymond, Monica L Marvin, et al.
Familial Cancer|October 8, 2014
Multiple skin hamartomata: a possible novel clinical presentation of SUFU neoplasia syndromeKirsty Mann, Jill Magee, Marine Guillaud-Bataille, et al.
Familial Cancer|September 18, 2014
Further evidence for pathogenicity of the TP53 tetramerization domain mutation p.Arg342Pro in Li-Fraumeni syndromeAnna Etzold, Julia C Schröder, Oliver Bartsch, et al.
Familial Cancer|July 25, 2013
Chemoprevention in Lynch syndromeJohn Burn, John C Mathers, D Tim Bishop
Familial Cancer|March 21, 2013
Psychosocial consequences of predictive genetic testing for Lynch syndrome and associations to surveillance behaviour in a 7-year follow-up studyKatja Aktan-Collan, Helena Kääriäinen, Heikki Järvinen, et al.
Familial Cancer|July 30, 2014
High-resolution melting (HRM) assay for the detection of recurrent BRCA1/BRCA2 germline mutations in Tunisian breast/ovarian cancer familiesAouatef Riahi, Maher Kharrat, Imen Lariani, et al.
Familial Cancer|August 31, 2013
Lynch Syndrome in high risk Ashkenazi Jews in IsraelYael Goldberg, Inbal Kedar, Revital Kariiv, et al.
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