| dc.creator |
Kuybulu, Ayca |
|
| dc.creator |
Sipahi, Tansu |
|
| dc.creator |
Akar, Nejat |
|
| dc.creator |
Karademir, Selmin |
|
| dc.date |
2009-11-01T01:00:00Z |
|
| dc.date.accessioned |
2021-12-03T11:30:30Z |
|
| dc.date.available |
2021-12-03T11:30:30Z |
|
| dc.identifier |
72e2f0b3-342e-449b-8a73-7f1c0728884d |
|
| dc.identifier |
10.1177/1076029608319883 |
|
| dc.identifier |
https://avesis.sdu.edu.tr/publication/details/72e2f0b3-342e-449b-8a73-7f1c0728884d/oai |
|
| dc.identifier.uri |
http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/92552 |
|
| dc.description |
A 2-year-old girl with tetralogy of Fallot presented with diffuse cranial infarct after cardiac angiography. Heterozygosity for factor V Leiden and prothrombin 20210A mutations were detected. The authors suggest that if thrombosis develops in patients with congenital heart disease, genetic risk factors should be evaluated. |
|
| dc.language |
eng |
|
| dc.rights |
info:eu-repo/semantics/closedAccess |
|
| dc.title |
Diffuse Cerebral Infarct Associated With Factor V Leiden and Prothrombin 20210A Mutations in a Patient With Tetralogy of Fallot |
|
| dc.type |
info:eu-repo/semantics/article |
|