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Familial Cancer|February 28, 2013
The InSiGHT database: utilizing 100 years of insights into Lynch syndromeJ P Plazzer, R H Sijmons, M O Woods, et al.Familial Cancer|March 12, 2013
Prevalence of HOXB13 mutation in a population of Ashkenazi Jewish men treated for prostate cancerShaheen Alanee, Sohela Shah, Joseph Vijai, et al.Familial Cancer|March 13, 2013
Novel and recurrent BRCA1/BRCA2 mutations in early onset and familial breast and ovarian cancer detected in the Program of Genetic Counseling in Cancer of Valencian Community (eastern Spain). Relationship of family phenotypes with mutation prevalenceInmaculada de Juan Jiménez, Zaida García Casado, Sarai Palanca Suela, et al.Familial Cancer|May 31, 2012
A multidisciplinary clinic for individualizing management of patients at increased risk for breast and gynecologic cancerNatalie J Engel, Patricia Gordon, Darcy L Thull, et al.Familial Cancer|May 31, 2012
The IL-10 promoter haplotype and cancer risk: evidence from a meta-analysisKui Zhang, Lushun Zhang, Xianmin Wang, et al.Familial Cancer|February 15, 2013
Mutation screening in a Norwegian cohort with pheochromocytomaWenche Sjursen, Henrik Halvorsen, Eva Hofsli, et al.Familial Cancer|November 27, 2012
An unusual BRCA mutation distribution in a high risk cancer genetics clinicAnna C Nelson-Moseke, Joanne M Jeter, Haiyan Cui, et al.Familial Cancer|April 5, 2013
Prediction models in Lynch syndromeFay Kastrinos, Judith Balmaña, Sapna SyngalFamilial Cancer|May 14, 2013
Phenotypic heterogeneity of hereditary gynecologic cancers: a report from the Creighton hereditary cancer registryMurray Joseph Casey, Chhanda Bewtra, Henry T Lynch, et al.Familial Cancer|June 18, 2013
Barrett's esophagus in the patients with familial adenomatous polyposisZoran Gatalica, Mingkui Chen, Carrie Snyder, et al.Pageof 152