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DE NOVO TERMINAL 4q DELETION SYNDROME WITH NEW OCULAR FINDINGS IN TURKISH TWINS: CASE REPORT

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dc.creator Ormeci, A. R.
dc.creator Oztas, S.
dc.creator Sandal, G.
dc.date 2013-01-01T01:00:00Z
dc.date.accessioned 2021-12-03T11:19:52Z
dc.date.available 2021-12-03T11:19:52Z
dc.identifier 3315ddf7-3672-44a2-8253-8f352396b13d
dc.identifier https://avesis.sdu.edu.tr/publication/details/3315ddf7-3672-44a2-8253-8f352396b13d/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/90794
dc.description De novo terminal 4q deletion syndrome with new ocular findings in Turkish twins: case report: The 4q deletion syndrome is a rare chromosome deletion syndrome with a wide range of clinical phenotypes. Herein we report cases of twins (karyotype 46, XY) carrying terminal deletion of the chromosome 4 (q3 lqter) segment resulting in craniofacial dysmorphism, skeletal anomalies, ocular findings and cardiac defect.
dc.language eng
dc.rights info:eu-repo/semantics/closedAccess
dc.title DE NOVO TERMINAL 4q DELETION SYNDROME WITH NEW OCULAR FINDINGS IN TURKISH TWINS: CASE REPORT
dc.type info:eu-repo/semantics/article


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