| 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 |
|