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Oxford University Press (OUP), Human Molecular Genetics, 12(2), p. 2099-2107

DOI: 10.1093/hmg/2.12.2099

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Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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