Zobrazeno 1 - 1
of 1
pro vyhledávání: '"Zulema Serrano Figueroa"'
Publikováno v:
Revista de Ciencias Médicas de Pinar del Río, Vol 21, Iss 6, Pp 955-959 (2017)
Introduction: Apert Syndrome is an autosomal dominant disorder, this defect is caused by a spontaneous mutation, which affects receptor 2 of the fibroblast growth factor. Case report: a case of Apert syndrome was presented in a patient whose disease
Externí odkaz:
https://doaj.org/article/a35312342b624a36bcb56ffa11d32798
