颅锁骨发育不全综合征2例病例报告及特征分析(2)
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参见附件。
89(5):773-779.
[2] Mundlos S. Cleidocranial dysplasia: Clinical and molecular gene-
tics[J]. J Med Genet, 1999, 36(3):177-182.
[3] Fernandez BA, Siegel-Bartelt J, Herbrick JA, et al. Holoprosen-
cephaly and cleidocranial dysplasia in a patient due to two posi-
tion-effect mutations: Case report and review of the literature[J].
Clin Genet, 2005, 68(4):349-359.
[4] 蒋兰, 李勇, 赖文莉. 锁骨颅骨发育不全综合征1例[J]. 华西口腔
医学杂志, 2009, 27(4):459-460.
Jiang Lan, Li Yong, Lai Wenli. Cleidocranial dysplasia: A case
report[J]. West China J Stomatol, 2009, 27(4):459-460.
[5] Lin WD, Lin SP, Wang CH, et al. RUNX2 mutations in Taiwanese
patients with cleidocranial dysplasia[J]. Genet Mol Biol, 2011, 34
(2):201-204.
[6] Zhang C, Zheng S, Wang Y, et al. Mutational analysis of RUNX2
gene in Chinese patients with cleidocranial dysplasia[J]. Mutage-
nesis, 2010, 25(6):589-594.
[7] Hermann NV, Hove HD, J?rgensen C, et al. Prenatal 3D ultra-
sound diagnostics in cleidocranial dysplasia[J]. Fetal Diagn Ther,2009, 25(1):36-39.
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