Transcript level alterations reflect gene dosage effects across multiple tissues in a mouse model of down syndrome
Human trisomy 21, which results in Down syndrome (DS), is one of the most complicated congenital genetic anomalies compatible with life, yet little is known about the molecular basis of DS. It is generally accepted that chromosome 21 (Chr21) transcripts are overexpressed by about 50% in cells with a...
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Veröffentlicht in: | Genome research 2004-07, Vol.14 (7), p.1258-1267 |
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