Zobrazeno 1 - 1
of 1
pro vyhledávání: '"Lisch sign"'
Publikováno v:
Türk Nöroloji Dergisi, Vol 14, Iss 4, Pp 277-283 (2008)
Scientific BACKGROUND: Neurofibromatosis is an autosomal dominant genetic disease which affects skin, nervous system and eyes. Neurofibromatosis has two frequently seen subtypes which are called Type 1 (Von Recklinghausen disease: periferal neurofibr
Externí odkaz:
https://doaj.org/article/da5f2a5a23f44268b2a7c9ebfb3cecd5
