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Familial Cancer|December 25, 2012
A de novo FLCN mutation in a patient with spontaneous pneumothorax and renal cancer; a clinical and molecular evaluationFred H Menko, Paul C Johannesma, R Jeroen A van Moorselaar, et al.
Familial Cancer|December 25, 2012
EPCAM deletion carriers constitute a unique subgroup of Lynch syndrome patientsMarjolijn J L Ligtenberg, Roland P Kuiper, Ad Geurts van Kessel, et al.
Familial Cancer|December 25, 2012
Unmet support needs and distress among women with a BRCA1/2 mutationAshley Farrelly, Victoria White, Bettina Meiser, et al.
Familial Cancer|January 5, 2013
Detection of large scale 3' deletions in the PMS2 gene amongst Colon-CFR participants: have we been missing anything?Mark Clendenning, Michael D Walsh, Judith Balmana Gelpi, et al.
Familial Cancer|December 11, 2012
A novel missense mutation (N78D) in a family with von Hippel-Lindau disease with central nervous system haemangioblastomas, pancreatic and renal cystsS Cingoz, R B van der Luijt, E Kurt, et al.
Familial Cancer|December 13, 2012
Frequency of 5382insC mutation of BRCA1 gene among breast cancer patients: an experience from Eastern IndiaAbhijit Chakraborty, Ashis Mukhopadhyay, Deboshree Bhattacharyya, et al.
Familial Cancer|January 12, 2013
Birt-Hogg-Dubé syndrome and the skinMarigje Vernooij, Tijs Claessens, Monique Luijten, et al.
Familial Cancer|December 1, 2012
A case of pneumatosis cystoides intestinalis mimicking familial adenomatous polyposisMaurizio Ponz de Leon, Claudia Bertarelli, Gian Piero Casadei, et al.
Familial Cancer|February 22, 2012
French women's breast self-examination practices with time after undergoing BRCA1/2 genetic testingC Maheu, T Apostolidis, A Petri-Cal, et al.
Familial Cancer|October 7, 2014
Long-term outcomes of risk-reducing surgery in unaffected women at increased familial risk of breast and/or ovarian cancerLouise Heiniger, Phyllis N Butow, Joseph Coll, et al.
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