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	1.	Transcriptomic analysis of skin in a case of ichthyosis Curth-Macklin caused by a KRT1 mutation. [electronic resource] by Ortega-Recalde, O Silgado, D Fetiva, C Fonseca, D J Laissue, P Producer: 20170918 In: The British journal of dermatology vol. 175 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Biallelic HERC1 mutations in a syndromic form of overgrowth and intellectual disability. [electronic resource] by Ortega-Recalde, O Beltrán, O I Gálvez, J M Palma-Montero, A Restrepo, C M Mateus, H E Laissue, P Producer: 20160627 In: Clinical genetics vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	A novel TGM1 mutation, leading to multiple splicing rearrangements, is associated with autosomal recessive congenital ichthyosis. [electronic resource] by Ortega-Recalde, O Moreno, M B Vergara, J I Fonseca, D J Rojas, R F Mosquera, H Medina, C L Restrepo, C M Laissue, P Producer: 20160623 In: Clinical and experimental dermatology vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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