Molecular cloning and expression analysis of a novel gene DGCR8 located in the DiGeorge syndrome chromosomal region

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Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.

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The DNA sequence of human chromosome 22

Ian Dunham, Adrienne Hunt, John Collins et al. · Nature · 1999 · 1.2K citations · Full text

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DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1

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Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice

Elizabeth A. Lindsay, Francesca Vitelli, Hong Hua Su et al. · Nature · 2001 · 1K citations

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