A genomic approach to study Down syndrome and cancer inverse comorbidity: Untangling the Chromosome 21

Down syndrome (DS), one of the most common birth defects and the most widespread genetic cause of intellectual disabilities, is caused by extra genetic material on chromosome 21 (HSA21). The increased genomic dosage of trisomy 21 is thought to be responsible for the distinct DS phenotypes, including...

Πλήρης περιγραφή

Λεπτομέρειες βιβλιογραφικής εγγραφής

Κύριοι συγγραφείς:	Jaume eForés-Martos, Raimundo eCervera-Vidal, Enrique Alejandro Chirivella Perez, Alberto eRamos-Jarero, Joan eCliment
Μορφή:	Artigo
Γλώσσα:	Inglês
Έκδοση:	Frontiers Media S.A. 2015-02-01
Σειρά:	Frontiers in Physiology
Θέματα:	Down Syndrome Cancer genomics RCAN1 21p11 Trisomy HSA21 Inverse comorbidity
Διαθέσιμο Online:	http://journal.frontiersin.org/Journal/10.3389/fphys.2015.00010/full
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