Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Satish K. Sundararajan"'
Publikováno v:
Journal of Neuroanaesthesiology and Critical Care, Vol 08, Iss 01, Pp 060-062 (2021)
Apert syndrome (AS) is an autosomal dominant disorder characterized by craniosynostosis, craniofacial anomalies, and symmetrical syndactyly of hands and feet. Ten percent children with AS can have associated congenital cardiac anomalies. Association
Externí odkaz:
https://doaj.org/article/ae830065d8934fb49675acbabe022c2b
Publikováno v:
Journal of Neuroanaesthesiology and Critical Care, Vol 08, Iss 01, Pp 060-062 (2021)
Apert syndrome (AS) is an autosomal dominant disorder characterized by craniosynostosis, craniofacial anomalies, and symmetrical syndactyly of hands and feet. Ten percent children with AS can have associated congenital cardiac anomalies. Association
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::901f944051566f6f2620d929b3edde22
http://www.thieme-connect.de/DOI/DOI?10.1055/s-0039-1692735
http://www.thieme-connect.de/DOI/DOI?10.1055/s-0039-1692735
Publikováno v:
20th Annual Conference of Indian Society of Neuroanaesthesiology and Critical Care (ISNACC).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6cf09253ef5a735516d973e264a66bec
https://doi.org/10.1055/s-0039-1684113
https://doi.org/10.1055/s-0039-1684113