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Hereditary Cancer in Clinical Practice|January 29, 2015
Molecular diagnosis and comprehensive treatment of multiple endocrine neoplasia type 2 in Southeastern ChineseJian-Qiang Zhao, Zhen-Guang Chen, Xiao-Ping Qi
Hereditary Cancer in Clinical Practice|January 22, 2015
PARP inhibitorsMaheen Anwar, Hafiz Muhammad Aslam, Shahzad Anwar
Hereditary Cancer in Clinical Practice|May 15, 2023
Size matters in telomere biology disorders ‒ expanding phenotypic spectrum in patients with long or short telomeresAnna Byrjalsen, Anna Engell Brainin, Thomas Kromann Lund, et al.
Hereditary Cancer in Clinical Practice|October 31, 2012
Diagnostic and pathogenetic role of café-au-lait macules in nevoid basal cell carcinoma syndromeGiovanni Ponti, Aldo Tomasi, Lorenza Pastorino, et al.
Hereditary Cancer in Clinical Practice|August 19, 2022
BRCA1/2 variants and copy number alterations status in non familial triple negative breast cancer and high grade serous ovarian cancerFatima Zahra El Ansari, Farah Jouali, Rim Fekkak, et al.
Hereditary Cancer in Clinical Practice|August 23, 2022
Barriers and facilitators to using aspirin for preventive therapy: a qualitative study exploring the views and experiences of people with Lynch syndrome and healthcare providersKelly E Lloyd, Robbie Foy, Louise H Hall, et al.
Hereditary Cancer in Clinical Practice|November 19, 2025
Contribution of MLH1, MSH2, and MSH6 large genomic rearrangements to Pakistani colorectal cancer patientsHumaira Naeemi, Noor Muhammad, Asif Loya, et al.
Hereditary Cancer in Clinical Practice|August 22, 2021
Myxofibrosarcoma harboring an MLH1 pathogenic germline variant associated with Muir-Torre syndrome: a case reportMakoto Nakagawa, Eisuke Kobayashi, Masayoshi Yamada, et al.
Hereditary Cancer in Clinical Practice|February 22, 2025
Analysis of informed consent forms of patients undergoing cancer genetic testing in the era of next-generation sequencingTina Kerševan, Tina Kogovšek, Ana Blatnik, et al.
Hereditary Cancer in Clinical Practice|February 21, 2025
De novo familial adenomatous polyposis with germline double heterozygosity of APC/BRCA2: a case report and literature reviewTian-Qi Zhang, Ji-Dong Cai, Cong Li, et al.
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