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...

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Үндсэн зохиолчид:	Jaume eForés-Martos, Raimundo eCervera-Vidal, Enrique Alejandro Chirivella Perez, Alberto eRamos-Jarero, Joan eCliment
Формат:	Artigo
Хэл сонгох:	Inglês
Хэвлэсэн:	Frontiers Media S.A. 2015-02-01
Цуврал:	Frontiers in Physiology
Нөхцлүүд:	Down Syndrome Cancer genomics RCAN1 21p11 Trisomy HSA21 Inverse comorbidity
Онлайн хандалт:	http://journal.frontiersin.org/Journal/10.3389/fphys.2015.00010/full
Шошгууд:	Шошго нэмэх Шошго байхгүй, Энэхүү баримтыг шошголох эхний хүн болох!