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  1. Article

    Open Access

    Partial trisomy 21 with or without highly restricted Down syndrome critical region (HR-DSCR): report of two new cases and reanalysis of the genotype–phenotype association

    Down syndrome (DS) is caused by the presence of an extra copy of full or partial human chromosome 21 (Hsa21). Partial (segmental) trisomy 21 (PT21) is the duplication of only a delimited region of Hsa21 and ca...

    Maria Chiara Pelleri, Chiara Locatelli, Teresa Mattina… in BMC Medical Genomics (2022)

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  2. Article

    Open Access

    The transcriptome profile of human trisomy 21 blood cells

    Trisomy 21 (T21) is a genetic alteration characterised by the presence of an extra full or partial human chromosome 21 (Hsa21) leading to Down syndrome (DS), the most common form of intellectual disability (ID...

    Francesca Antonaros, Rossella Zenatelli, Giulia Guerri, Matteo Bertelli… in Human Genomics (2021)

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