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Familial Cancer|August 4, 2020
Characterizing germline APC and MUTYH variants in Ashkenazi Jews compared to other individualsChinedu Ukaegbu, Zohar Levi, Tara D Fehlmann, et al.
Familial Cancer|August 10, 2020
Is a colorectal neoplasm diagnosis a trigger to change dietary and other lifestyle habits for persons with Lynch syndrome? A prospective cohort studyJesca G M Brouwer, Merel Snellen, Tanya M Bisseling, et al.
Familial Cancer|March 28, 2015
Germline mutations predisposing to non-small cell lung cancerGerald H Clamon, Aaron D Bossler, Taher Abu Hejleh, et al.
Familial Cancer|April 6, 2015
Specific Alu elements involved in a significant percentage of copy number variations of the STK11 gene in patients with Peutz-Jeghers syndromePawel Borun, Marina De Rosa, Boguslaw Nedoszytko, et al.
Familial Cancer|February 26, 2015
Heterozygous germline mutations in NBS1 among Korean patients with high-risk breast cancer negative for BRCA1/2 mutationHaeyoung Kim, Dae-Yeon Cho, Doo Ho Choi, et al.
Familial Cancer|February 27, 2015
Mutations of HNRNPA0 and WIF1 predispose members of a large family to multiple cancersChongjuan Wei, Bo Peng, Younghun Han, et al.
Familial Cancer|April 4, 2015
Risk factors for endometrial cancer among women with a BRCA1 or BRCA2 mutation: a case control studyYakir Segev, Barry Rosen, Jan Lubinski, et al.
Familial Cancer|March 11, 2015
Genetic screening in patients with Retinoblastoma in IsraelMichal Sagi, Avishag Frenkel, Avital Eilat, et al.
Familial Cancer|August 18, 2020
Clinical phenotypes combined with saturation genome editing identifying the pathogenicity of BRCA1 variants of uncertain significance in breast cancerQiting Wan, Li Hu, Tao Ouyang, et al.
Familial Cancer|April 3, 2021
Constitutional 2p16.3 deletion including MSH6 and FBXO11 in a boy with developmental delay and diffuse large B-cell lymphomaN van Engelen, F van Dijk, E Waanders, et al.
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