The transcriptome profile of human trisomy 21 blood cells

BACKGROUND: 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). It is broadly agreed that the presence of extra genetic material in T21 give...

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Bibliografiska uppgifter
I publikationen:Hum Genomics
Huvudupphovsmän: Antonaros, Francesca, Zenatelli, Rossella, Guerri, Giulia, Bertelli, Matteo, Locatelli, Chiara, Vione, Beatrice, Catapano, Francesca, Gori, Alice, Vitale, Lorenza, Pelleri, Maria Chiara, Ramacieri, Giuseppe, Cocchi, Guido, Strippoli, Pierluigi, Caracausi, Maria, Piovesan, Allison
Materialtyp: Artigo
Språk:Inglês
Publicerad: BioMed Central 2021
Ämnen:
Primary Research
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC8088681/
https://ncbi.nlm.nih.gov/pubmed/33933170
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40246-021-00325-4
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