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3. Congenital ichthyosis in Prader–Willi syndrome associated with maternal chromosome 15 uniparental disomy: Case report and review of autosomal recessive conditions unmasked by UPD. Issue 10 (20th August 2020)

7. Ichthyosis prematurity syndrome mimics keratitis–ichthyosis–deafness syndrome at birth: Use of electron microscopy and genetic testing. (4th September 2015)