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Volumn 36, Issue 3, 2008, Pages 188-189

Fine-needle aspiration cytological features of cherubism

Author keywords

Cherubism; FNA; Giant cell lesions

Indexed keywords

ADOLESCENT; ARTICLE; ASPIRATION BIOPSY; ASPIRATION CYTOLOGY; CASE REPORT; CELL STRUCTURE; CLINICAL EXAMINATION; FIBROUS DYSPLASIA; GIANT CELL; HUMAN; HUMAN TISSUE; MALE; MAXILLA; OSTEOCLAST; PRIORITY JOURNAL;

EID: 39749179179     PISSN: 87551039     EISSN: 10970339     Source Type: Journal    
DOI: 10.1002/dc.20791     Document Type: Article
Times cited : (8)

References (6)
  • 1
  • 2
    • 0029153893 scopus 로고
    • Spontaneous deletion in the FMR1 gene in a patient with fragile X syndrome and cherubism
    • Quan F, Grompe M, Jakobs P, Popovich BW. Spontaneous deletion in the FMR1 gene in a patient with fragile X syndrome and cherubism. Hum Mol Genet 1995;4:1681-1684.
    • (1995) Hum Mol Genet , vol.4 , pp. 1681-1684
    • Quan, F.1    Grompe, M.2    Jakobs, P.3    Popovich, B.W.4
  • 6
    • 0242426493 scopus 로고    scopus 로고
    • A missense mutation in the SH3BP2 gene on chromosome 4p16.3 found in a case of nonfamilial cherubism
    • Imai Y, Kanno K, Moriya T, et al. A missense mutation in the SH3BP2 gene on chromosome 4p16.3 found in a case of nonfamilial cherubism. Cleft Palate Craniofac J 2003;40:632-638.
    • (2003) Cleft Palate Craniofac J , vol.40 , pp. 632-638
    • Imai, Y.1    Kanno, K.2    Moriya, T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.