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1.
Verheije, R.* et al.: Heterozygous loss-of-function variants of MEIS2 cause a triad of palatal defects, congenital heart defects, and intellectual disability. Eur. J. Hum. Genet. 27, 278-290 (2019)
2.
Koolen, D.A.* et al.: Clinical and molecular delineation of the 17q21.31 microdeletion syndrome. J. Med. Genet. 45, 710-720 (2008)
3.
Ross, M.T.* et al.: The DNA sequence of the human X chromosome. Nature 434, 325-337 (2005)