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	1.	Whole-exome sequencing identifies a novel missense mutation in EDAR causing autosomal recessive hypohidrotic ectodermal dysplasia with bilateral amastia and palmoplantar hyperkeratosis. [electronic resource] by Haghighi, A Nikuei, P Haghighi-Kakhki, H Saleh-Gohari, N Baghestani, S Krawitz, P M Hecht, J Mundlos, S Producer: 20140227 In: The British journal of dermatology vol. 168 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Identification of a founder mutation in KRT14 associated with Naegeli-Franceschetti-Jadassohn syndrome. [electronic resource] by Ralser, D J Kumar, S Borisov, O Sarig, O Richard, G Wolf, S Krawitz, P M Sprecher, E Kreiß, M Betz, R C Producer: 20210514 In: The British journal of dermatology vol. 183 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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