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Hereditary Cancer in Clinical Practice|September 28, 2024
PMS2 mutation spectra in Norway and risk of cancer for carriers of pathogenic variantsWenche Sjursen, Hanne K Hyldebrandt, Liss Anne S Lavik, et al.
Hereditary Cancer in Clinical Practice|September 19, 2024
Blood molybdenum level as a marker of cancer risk on BRCA1 carriersMilena Matuszczak, Adam Kiljańczyk, Wojciech Marciniak, et al.
Hereditary Cancer in Clinical Practice|February 18, 2025
Assessing germline TP53 mutations in cancer patients: insights into Li-Fraumeni syndrome and genetic testing guidelinesAnastasiia Danishevich, Daria Fedorova, Natalia Bodunova, et al.
Hereditary Cancer in Clinical Practice|August 19, 2024
Benefits of osimertinib treat a lung adenocarcinoma patient with germline EGFR T790M, somatic EGFR 19-Del, TP53 and PIK3CA mutationsYingxue Li, Guangqi Li, Zheng Zheng, et al.
Hereditary Cancer in Clinical Practice|January 25, 2019
Implementation of massive sequencing in the genetic diagnosis of hereditary cancer syndromes: diagnostic performance in the Hereditary Cancer Programme of the Valencia Community (FamCan-NGS)Marta Ramírez-Calvo, Zaida García-Casado, Antonio Fernández-Serra, et al.
Hereditary Cancer in Clinical Practice|July 22, 2021
Expanding the phenotype of E318K (c.952G > A) MITF germline mutation carriers: case series and review of the literatureLeandro Jonata Carvalho Oliveira, Aline Bobato Lara Gongora, Fabiola Ambrosio Silveira Lima, et al.
Hereditary Cancer in Clinical Practice|December 14, 2020
Characteristics and genetic testing outcomes of patients with clinically suspected paraganglioma/pheochromocytoma (PGL/PCC) syndrome in SingaporeKay Reen Ting, Pei Yi Ong, Samuel Ow Guan Wei, et al.
Hereditary Cancer in Clinical Practice|January 7, 2021
Revisiting multiple erroneous genetic testing results and clinical misinterpretations in a patient with Li-Fraumeni syndrome: lessons for translational medicineTatiana N Sokolova, Valeriy V Breder, Irina S Shumskaya, et al.
Hereditary Cancer in Clinical Practice|June 18, 2013
Carcinogenesis of PIK3CASidra German, Hafiz Muhammad Aslam, Shafaq Saleem, et al.
Hereditary Cancer in Clinical Practice|July 9, 2013
Sense of coherence and self-concept in Lynch syndromeHelle Vendel Petersen, Steen Ladelund, Christina Carlsson, et al.
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