Zobrazeno 1 - 1
of 1
pro vyhledávání: '"Céleste Koval"'
Autor:
Christine Bodemer, Laurence Jonard, Sylvie Freitag, M'hamed Grati, Delphine Feldmann, Rémy Couderc, Céleste Koval, Françoise Denoyelle, Martine Sinico, Sandrine Marlin, Smail Hadj-Rabia, Christophe Parsy
Publikováno v:
European Journal of Medical Genetics. 51:35-43
Keratitis-Ichthyosis-Deafness (KID) syndrome (OMIM 148210) is a congenital ectodermal defect. KID consists of an atypical ichthyosiform erythroderma associated with congenital sensorineural deafness. A rare form of the KID syndrome is a fatal course
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee5315991bdba727a663ba13451d50aa
https://doi.org/10.1016/j.ejmg.2007.09.005
https://doi.org/10.1016/j.ejmg.2007.09.005
