EN
TR
Benign chondroblastoma (a case report)
Öz
Chondroblastoma is a rare benign primary bone neoplasm. The clinical symptoms are generally including adjacent joint because of the lesion arises in the epiphysis of long bones. In this report; a case of chondroblastoma is discussed which was considered to be "Tear of Medial Meniscus" clinically.
Anahtar Kelimeler
Ayrıntılar
Birincil Dil
İngilizce
Konular
-
Bölüm
-
Yayımlanma Tarihi
11 Eylül 2006
Gönderilme Tarihi
6 Mart 2014
Kabul Tarihi
-
Yayımlandığı Sayı
Yıl 1993 Cilt: 27 Sayı: 3
APA
Gulman, B., & Ciray, M. (2006). Benign chondroblastoma (a case report). Acta Orthopaedica et Traumatologica Turcica, 27(3), 197-199. https://doi.org/10.3944/aott.v27i3.1412
AMA
1.Gulman B, Ciray M. Benign chondroblastoma (a case report). Acta Orthopaedica et Traumatologica Turcica. 2006;27(3):197-199. doi:10.3944/aott.v27i3.1412
Chicago
Gulman, Birol, ve Mevlut Ciray. 2006. “Benign chondroblastoma (a case report)”. Acta Orthopaedica et Traumatologica Turcica 27 (3): 197-99. https://doi.org/10.3944/aott.v27i3.1412.
EndNote
Gulman B, Ciray M (01 Eylül 2006) Benign chondroblastoma (a case report). Acta Orthopaedica et Traumatologica Turcica 27 3 197–199.
IEEE
[1]B. Gulman ve M. Ciray, “Benign chondroblastoma (a case report)”, Acta Orthopaedica et Traumatologica Turcica, c. 27, sy 3, ss. 197–199, Eyl. 2006, doi: 10.3944/aott.v27i3.1412.
ISNAD
Gulman, Birol - Ciray, Mevlut. “Benign chondroblastoma (a case report)”. Acta Orthopaedica et Traumatologica Turcica 27/3 (01 Eylül 2006): 197-199. https://doi.org/10.3944/aott.v27i3.1412.
JAMA
1.Gulman B, Ciray M. Benign chondroblastoma (a case report). Acta Orthopaedica et Traumatologica Turcica. 2006;27:197–199.
MLA
Gulman, Birol, ve Mevlut Ciray. “Benign chondroblastoma (a case report)”. Acta Orthopaedica et Traumatologica Turcica, c. 27, sy 3, Eylül 2006, ss. 197-9, doi:10.3944/aott.v27i3.1412.
Vancouver
1.Birol Gulman, Mevlut Ciray. Benign chondroblastoma (a case report). Acta Orthopaedica et Traumatologica Turcica. 01 Eylül 2006;27(3):197-9. doi:10.3944/aott.v27i3.1412