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Familial Cancer|February 20, 2016
Familial atypical multiple mole melanoma (FAMMM) syndrome: history, genetics, and heterogeneityHenry T Lynch, Trudy G Shaw
Familial Cancer|June 24, 2018
Capillary electrophoresis as alternative method to detect tumor genetic mutations: the model built on the founder BRCA1 c.4964_4982del19 variantMaria De Bonis, Angelo Minucci, Giovanni Luca Scaglione, et al.
Familial Cancer|January 17, 2017
Baseline results from the UK SIGNIFY study: a whole-body MRI screening study in TP53 mutation carriers and matched controlsSibel Saya, Emma Killick, Sarah Thomas, et al.
Familial Cancer|August 23, 2019
Population frequencies of pathogenic alleles of BRCA1 and BRCA2: analysis of 173 Danish breast cancer pedigrees using the BOADICEA modelThorkild Terkelsen, Lise-Lotte Christensen, Deirdre Cronin Fenton, et al.
Familial Cancer|February 24, 2019
Progress report: familial pancreatic cancerIoannis Mintziras, Detlef K Bartsch
Familial Cancer|March 12, 2017
Lower gastrointestinal neuroendocrine neoplasms associated with hereditary cancer syndromes: a case seriesTrilokesh D Kidambi, Christina Pedley, Amie Blanco, et al.
Familial Cancer|March 13, 2017
Improved quality of risk-reducing salpingo-oophorectomy in Australasian women at high risk of pelvic serous cancerY C Lee, M Bressel, P Grant, et al.
Familial Cancer|October 24, 2003
Familial adenomatous polyposis at the Tel Aviv Medical Center: demographic and clinical featuresP Rozen, Z Samuel, M Rabau, et al.
Familial Cancer|October 24, 2003
FAP associated thyroid carcinoma in mother and her daughterK Kameyama, H Takami
Familial Cancer|October 24, 2003
Mutations of the 'minor' mismatch repair gene MSH6 in typical and atypical hereditary nonpolyposis colorectal cancerE Lucci-Cordisco, V Rovella, S Carrara, et al.
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