Associated Papers
Cancer of Unknown Primary (CUP): genetic evidence for a novel nosological entity? A case report.
Benvenuti S et al.
Embo Molecular Medicine, 2020
32511869 (PubMed )
Supplement: EMMM-12-e11756-s005.xlsx › Sheet_1
Exome sequencing identifies potential risk variants for Mendelian disorders at high prevalence in Qatar.
Rodriguez-Flores JL et al.
Human Mutation, 2014
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