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Familial Cancer|December 10, 2009
Biallelic MYH germline mutations as cause of Muir-Torre syndromeCarmen Guillén-Ponce, Adela Castillejo, Víctor M Barberá, et al.
Familial Cancer|December 13, 2005
BAP1 and breast cancer riskIsabelle Coupier, Pierre-Yves Cousin, David Hughes, et al.
Familial Cancer|December 13, 2005
Patient satisfaction of BRCA1/2 genetic testing by women at high risk for breast cancer participating in a prevention trialJennifer R Klemp, Anne O'Dea, Carolyn Chamberlain, et al.
Familial Cancer|December 13, 2005
Survival of patients with ovarian cancer due to a mismatch repair defectTh E M Crijnen, M L G Janssen-Heijnen, H Gelderblom, et al.
Familial Cancer|December 13, 2005
Lack of germ-line mutations at the specific BRCA1-IRIS coding sequence in 114 Spanish high-risk breast/ovarian familiesMiguel de la Hoya, Juan Manuel Fernández, Ana Sánchez de Abajo, et al.
Familial Cancer|January 8, 2010
A new familial cancer syndrome including predisposition to Wilms tumor and neuroblastomaFatemeh Abbaszadeh, Karen T Barker, Carmel McConville, et al.
Familial Cancer|November 18, 2017
SNP association study in PMS2-associated Lynch syndromeSanne W Ten Broeke, Fadwa A Elsayed, Lisa Pagan, et al.
Familial Cancer|November 11, 2017
Genotype phenotype correlation in Asian Indian von Hippel-Lindau (VHL) syndrome patients with pheochromocytoma/paragangliomaNilesh Lomte, Sanjeet Kumar, Vijaya Sarathi, et al.
Familial Cancer|November 11, 2017
Excluding Lynch syndrome in a female patient with metachronous DNA mismatch repair deficient colon- and ovarian cancerStijn Crobach, Anne M L Jansen, Marjolein J L Ligtenberg, et al.
Familial Cancer|March 29, 2018
Germline CDH1 mutations are a significant contributor to the high frequency of early-onset diffuse gastric cancer cases in New Zealand MāoriChristopher Hakkaart, Lis Ellison-Loschmann, Robert Day, et al.
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