Zobrazeno 1 - 1
of 1
pro vyhledávání: '"Serdar Köseoğlu"'
Publikováno v:
Gaziantep Medical Journal. 19:191
Apert syndrome is a rare, autosomal dominantly inherited disease characterized by irregular craniosynostosis and some malformations involving face, hands and feet. Respiratory functions are frequently deteriorated due to hypoplasia of oropharyngeal a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6560fedb2215ceff57e76e19bf70dc1
https://doi.org/10.5455/gmj-30-2013-141
https://doi.org/10.5455/gmj-30-2013-141
