Author:
Barruet K.,Saka B.,Kombaté K.,Mouhari-Toure A.,Nguepmeni Noune J.,Akakpo S.,Tchangaï-Walla K.,Pitché P.
Reference12 articles.
1. A case of generalized congenital keratoderma with unusual involvement of 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. Missense mutations in GJB2 encoding connexin 26 cause the ectodermal dysplasia keratitis-ichthyosis-deafnes syndrome;Richard;Am J Hum Genet,2002
4. KID syndrome : une cause de pachydermatoglyphie;Boudghene Stambouli;Ann Dermatol Venereol,2003
5. Keratitis, ichthyosis and deafness syndrome with development of multiple hair follicle tumours;Kim;Br J Dermatol,2002
Cited by
2 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献