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  1. Article

    Open Access

    A map of copy number variations in the Tunisian population: a valuable tool for medical genomics in North Africa

    Copy number variation (CNV) is considered as the most frequent type of structural variation in the human genome. Some CNVs can act on human phenotype diversity, encompassing rare Mendelian diseases and genomic...

    Lilia Romdhane, Nessrine Mezzi, Hamza Dallali, Olfa Messaoud… in npj Genomic Medicine (2021)

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