Associated Papers
Multi-locus inherited neoplasia alleles syndromes in cancer: implications for clinical practice.
Yuen J et al.
European Journal of Human Genetics : Ejhg, 2025
39843919 (PubMed )
Supplement: 41431_2025_1785_MOESM2_ESM.pdf
Succinate dehydrogenase variants in paraganglioma: why are B subunit variants 'bad'?
Gruber LM et al.
Endocrine Oncology (bristol, England), 2023
37434649 (PubMed )
Supplement: supplementary_table_1.xlsx › Truncating_Variants
Clinical relevance of screening checklists for detecting cancer predisposition syndromes in Asian childhood tumours.
Chan SH et al.
Npj Genomic Medicine, 2018
Clinical management of pheochromocytoma and paraganglioma in Singapore: missed opportunities for genetic testing.
Chew WHW et al.
Molecular Genetics & Genomic Medicine, 2017
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