CHILD syndrome caused by a deletion of exons 6-8 of the NSDHL gene.
Kim CA; Konig A; Bertola DR; Albano LM; Gattás GJ; Bornholdt D; Leveleki L; Happle R; Grzeschik KH; Dermatology (Basel, Switzerland), 2005, vol. 211, issue 2, p 155, ISSN 10188665. ISBN 10188665.

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