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Contiguous gene syndrome due to a maternally inherited 8.41 Mb distal deletion of chromosome band Xp22.3 in a boy with short stature, ichthyosis, epilepsy, mental retardation, cerebral cortical heterotopias and Dandy-Walker malformation.
van Steensel MA, Vreeburg M, Engelen J, Ghesquiere S, Stegmann AP, Herbergs J, van Lent J, Smeets B, Vles JH. van Steensel MA, et al. Among authors: vles jh. Am J Med Genet A. 2008 Nov 15;146A(22):2944-9. doi: 10.1002/ajmg.a.32473. Am J Med Genet A. 2008. PMID: 18925676
[Main points and concerns in plagiocephaly].
Ruige M, Palmans EJ, Vles JH. Ruige M, et al. Among authors: vles jh. Tijdschr Kindergeneeskd. 1993 Feb;61(1):24-7. Tijdschr Kindergeneeskd. 1993. PMID: 8493699 Dutch.