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Crouzon 증후군 환자의 증례보고' 의 주제별 논문영향력
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Crouzon 증후군 환자의 증례보고' 의 참고문헌
Undiagnosed obstructive sleep apnea syndrome in children with syndromal craniofacial synostosis
The craniofacial dysostosis syndromes; current surgical thinking and future directions
Syndromes with craniostenosinostopsys; general aspects and well-known syndromes
Physical and oral characteristics of Crouzon syndrome, Apert syndrome and Pierre Robin sequence
Oral health status of children with syndromic craniosynostosis
Morphology and growth of the mandible in Crouzon, Apert, and Pfeiffer syndromes
Midface anomalies in children
Lefort III advancement with and without osteogenesis distraction
Is craniofacial morphology in Apert and Crouzon syndromes the same?
Dysostosis carnio-faciale hereditaire
Dentofacial features of a family with Crouzon syndrome; case reports
Crouzon syndrome; cephalometric analysis and evaluation of pathogenesis
Crouzon disease-a case report
Crouzon Syndrome; a clinical and roentgencephalometric study
Craniosynostosis syndromes; from genes to premature fusion of skull bones
Clinically mild, atypical, and aged craniofacial syndrome is diagnosed as Crouzon syndrome by identification of a point mutation in the fibroblast growth factor receptor 2 gene (FGFR2)
Apert and Crouzon syndromes; clinical findings, genes and extracellular matrix
A further mutation of the FGFR2 tyrosine kinase domain in mild Crouzon syndrome
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Crouzon 증후군 환자의 증례보고'
의 유사주제(
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