Congenital Reticular Ichthyosiform Erythroderma V. Dvorakova, RM Watson, A. Terron–Kwiatkowski, N. Andrew and AD. Irvine 1Depa
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Ichthyosis with confetti: clinics, molecular genetics and management | Orphanet Journal of Rare Diseases | Full Text
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Clinical and genetic findings in 13 Chinese children with keratinopathic ichthyosis | Pediatric Investigation
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Clinical examples of patients with congenital reticular ichthyosiform... | Download Scientific Diagram
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IJMS | Free Full-Text | First Case of KRT2 Epidermolytic Nevus and Novel Clinical and Genetic Findings in 26 Italian Patients with Keratinopathic Ichthyoses
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Mitotic recombination in patients with ichthyosis causes reversion of dominant mutations in KRT10. - Abstract - Europe PMC
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Ichthyosis with confetti: clinics, molecular genetics and management | Orphanet Journal of Rare Diseases | Full Text
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PDF] The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3 ′ End of KRT 10 FromDisease to a Syndrome | Semantic Scholar
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PDF] Expanding the Clinical and Genetic Spectrum of KRT1, KRT2 and KRT10 Mutations in Keratinopathic Ichthyosis. | Semantic Scholar
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Coexistence of mutations in keratin 10 (KRT10) and the mitochondrial genome in a patient with ichthyosis with confetti and Leber's hereditary optic neuropathy - Kalinska‐Bienias - 2017 - American Journal of Medical
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Mitotic Recombination in Patients with Ichthyosis Causes Reversion of Dominant Mutations in KRT10 | Science
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IAMA person with a severe form of ichthyosis, often talked about on r/WTF. Pictures of my skin inside. AMA. : r/IAmA
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