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A Korean Family with the Muenke Syndrome

The Muenke syndrome (MS) is characterized by unicoronal or bicoronal craniosynostosis, midfacial hypoplasia, ocular hypertelorism, and a variety of minor abnormalities associated with a mutation in the fibroblast growth factor receptor 3 (FGFR3) gene. The birth prevalence is approximately one in 10,...

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Detalles Bibliográficos
Autores principales:	Yu, Jae Eun, Park, Dong Ha, Yoon, Soo Han
Formato:	Texto
Lenguaje:	English
Publicado:	The Korean Academy of Medical Sciences 2010
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2890890/ https://www.ncbi.nlm.nih.gov/pubmed/20592905 http://dx.doi.org/10.3346/jkms.2010.25.7.1086

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