Intragenic microdeletion of RUNX2 is a novel mechanism for cleidocranial dysplasia.
about
RUNX2 mutations in Taiwanese patients with cleidocranial dysplasiaMolecular genetics of supernumerary tooth formation.Cleidocranial dysplasia presenting with retained deciduous teeth in a 15-year-old girl: a case report.RUNX2 mutations in Chinese patients with cleidocranial dysplasia.Cleidocranial dysplasia and RUNX2-clinical phenotype-genotype correlation.Genetic alterations in mesiodens as revealed by targeted next-generation sequencing and gene co-occurrence network analysis.Restorative treatment strategies for patients with cleidocranial dysplasia.Severe cleidocranial dysplasia and hypophosphatasia in a child with microdeletion of the C-terminal region of RUNX2.Patients with isolated oligo/hypodontia caused by RUNX2 duplication.
P2860
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P2860
Intragenic microdeletion of RUNX2 is a novel mechanism for cleidocranial dysplasia.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
Intragenic microdeletion of RUNX2 is a novel mechanism for cleidocranial dysplasia.
@en
type
label
Intragenic microdeletion of RUNX2 is a novel mechanism for cleidocranial dysplasia.
@en
prefLabel
Intragenic microdeletion of RUNX2 is a novel mechanism for cleidocranial dysplasia.
@en
P2093
P2860
P1433
P1476
Intragenic microdeletion of RUNX2 is a novel mechanism for cleidocranial dysplasia.
@en
P2093
Anne Chun-Hui Tsai
Chih-Yang Liu
Ching-Heng Chou
Chyi-Chyang Lin
Feng-Mei Sun
Fuu-Jen Tsai
Jer-Yuarn Wu
Li-Chen Huang
Ming Ta Michael Lee
Pauline Yen
P2860
P356
10.1007/S11568-008-9024-Y
P577
2008-01-01T00:00:00Z