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Hereditary Cancer in Clinical Practice|May 3, 2016
Assessing biases of information contained in pedigrees for the classification of BRCA-genetic variants: a study arising from the ENIGMA analytical working groupC H H Kerkhofs, A B Spurdle, P J Lindsey, et al.
Hereditary Cancer in Clinical Practice|June 16, 2022
Spectrum of germline pathogenic variants using a targeted next generation sequencing panel and genotype-phenotype correlations in patients with suspected hereditary breast cancer at an academic medical centre in PakistanFizza Akbar, Zahraa Siddiqui, Muhammad Talha Waheed, et al.
Hereditary Cancer in Clinical Practice|July 8, 2021
Ultrasound guided needle biopsy of axilla to evaluate nodal metastasis after preoperative systemic therapy in cohort of 106 breast cancers enriched with BRCA1/2 pathogenic variant carriersBaiba Līcīte, Arvīds Irmejs, Jeļena Maksimenko, et al.
Hereditary Cancer in Clinical Practice|October 28, 2020
Biological and clinical impact of central nervous system hemangioblastomas in Chinese patients with von Hippel-Lindau disease: implications for treatmentZhen Liu, Liang Li, Zhiqiang Yi, et al.
Hereditary Cancer in Clinical Practice|October 28, 2020
An in-depth exploration of the post-test informational needs of BRCA1 and BRCA2 pathogenic variant carriers in AsiaJeanette Yuen, Si Ming Fung, Chin Leong Sia, et al.
Hereditary Cancer in Clinical Practice|November 21, 2022
The Prospective Lynch Syndrome Database: background, design, main results and complete MySQL codePål Møller
Hereditary Cancer in Clinical Practice|January 20, 2021
A rare large duplication of MLH1 identified in Lynch syndromeAbhishek Kumar, Nagarajan Paramasivam, Obul Reddy Bandapalli, et al.
Hereditary Cancer in Clinical Practice|January 20, 2021
Novel PHOX2B germline mutation in childhood medulloblastoma: a case reportCaiping Ke, Xiaoshun Shi, Allen Menglin Chen, et al.
Hereditary Cancer in Clinical Practice|January 20, 2021
Recontacting non-BRCA1/2 breast cancer patients for germline CHEK2 c.1100del pathogenic variant testing: uptake and patient experiencesMary E Velthuizen, Rob B van der Luijt, Beja J de Vries, et al.
Hereditary Cancer in Clinical Practice|March 13, 2019
BRACAVENIR: an observational study of expectations and coping in young women with high hereditary risk of breast and ovarian cancerFabrice Kwiatkowski, Mathilde Gay-Bellile, Pascal Dessenne, et al.
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