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Novel chromosomal microduplications associated with dolichocephaly craniosynostosis: A case report

INSTRUCTION: Craniosynostosis is a human disorder characterized by the premature fusing of the cranial sutures in infants. Point mutations in hotspot genes such as FGFRs are the well-recognized causes of syndromic craniosynostosis, but chromosomal abbreviations may also play an important role in dev...

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Detalles Bibliográficos
Autores principales:	Yu, Dongyi, Li, Shuo, Liu, Qi, Zhang, Kai
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer Health 2017
Materias:	3500
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5728844/ https://www.ncbi.nlm.nih.gov/pubmed/29245229 http://dx.doi.org/10.1097/MD.0000000000008729

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