Publications by authors named "Giulia Rollo"

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Validation of the NovaSeq6000 platform and automated library preparation for CE-IVD equivalence.
Elena Pasquinelli, Giulia Rollo, Flavia Tinella, Miriana Danelli, Samantha Minetto

Comput Struct Biotechnol J· November 2025

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Slowly progressive autosomal dominant Alport Syndrome due to COL4A3 splicing variant.
Sergio Daga, Lorenzo Loberti, Giulia Rollo, Loredaria Adamo, Olga Lorenza Colavecchio

Eur J Hum Genet· April 2025

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Correction: Slowly progressive autosomal dominant Alport Syndrome due to COL4A3 splicing variant.
Sergio Daga, Lorenzo Loberti, Giulia Rollo, Loredaria Adamo, Olga Lorenza Colavecchio

Eur J Hum Genet· April 2025

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