Author:
Cheung Albert Y.,Patel Sunny,Kurji Khaliq H.,Sarnicola Enrica,Eslani Medi,Govil Amit,Holland Edward J.
Publisher
Ovid Technologies (Wolters Kluwer Health)
Reference13 articles.
1. A case of generalized congenital keratoderma, with unusual involvement of the eyes, ears, and nasal and buccal mucous membranes;Burns;J Cutan Dis.,1915
2. The keratitis, ichthyosis, and deafness (KID) syndrome;Skinner;Arch Dermatol.,1981
3. Ocular manifestations of keratitis-ichthyosis-deafness (KID) syndrome;Messmer;Ophthalmology.,2005
4. Keratitis, hepatitis, ichthyosis, and deafness: report and review of KID syndrome;Wilson;Am J Med Genet.,1991
5. De novo mutation in the gene encoding connexin-26 (GJB2) in a sporadic case of keratitis-ichthyosis-deafness (KID) syndrome;Alvarez;Am J Med Genet.,2003
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