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Oral-Facial-Digital Syndrome Type 1: Oral Findings in a 6-Year-Old Girl

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dc.creator ÖZ, Esra
dc.creator KIRZIOĞLU, Zühal
dc.date 2018-05-31T21:00:00Z
dc.date.accessioned 2020-10-06T11:22:29Z
dc.date.available 2020-10-06T11:22:29Z
dc.identifier c207eddd-e869-4b7c-8e64-99d584627e96
dc.identifier 10.1055/s-0037-1618601
dc.identifier https://avesis.sdu.edu.tr/publication/details/c207eddd-e869-4b7c-8e64-99d584627e96/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/71239
dc.description Oral-facial-digital syndrome (OFDS) is a group of congenital anomalies with 13 different forms. OFDS type 1 (OFDS1) is a developmental genetic anomaly related to the X chromosome, that is often seen in girls, and affects the face, oral cavity, and extremities. In this study, we discuss the oral findings of a 6-year-old girl with OFDS1 and her situation after 2.5 years.
dc.language eng
dc.rights info:eu-repo/semantics/closedAccess
dc.title Oral-Facial-Digital Syndrome Type 1: Oral Findings in a 6-Year-Old Girl
dc.type info:eu-repo/semantics/article


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