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1.8 Microdeletion and microduplication in 10q11.22

To date, interstitial deletions involving 10q11.2 have been reported in over 40 patients with variable abnormal phenotypes but also in individuals with a normal phenotype. The only clinical features common to a majority of affected individuals [were ID and DD.]

To date, interstitial deletions involving 10q11.2 have been reported in over 10 patients with variable abnormal phenotypes, individuals with a normal phenotype, and two prenatal cases, one with a normal and the other with an abnormal phenotype [Bisgaard et al., 2007; Fewtrell et al., 1994; Fryns et al., 1991; Ghai et al., 2011; Holden and MacDonald, 1985; Kirchhoff et al., 2005; Lobo et al., 1992; Shapiro et al., 1985; Zenger-Hain et al., 1993].
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The source is mentioned right after the documented passage.

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