A new phenotypic variant in cleidocranial dysplasia (CCD) associated with mutation c.391C>T of the RUNX2 gene.
about
Antagonistic Functions of USAG-1 and RUNX2 during Tooth DevelopmentDirect Delivery of Recombinant Pin1 Protein Rescued Osteoblast Differentiation of Pin1-Deficient Cells.Acute myeloid leukemia in a 3 years old child with cleidocranial dysplasiaIdentification of a novel mutation of RUNX2 in a family with supernumerary teeth and craniofacial dysplasia by whole-exome sequencing: A case report and literature review
P2860
A new phenotypic variant in cleidocranial dysplasia (CCD) associated with mutation c.391C>T of the RUNX2 gene.
description
2012 nî lūn-bûn
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2012年の論文
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2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
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2012年论文
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name
A new phenotypic variant in cl ...... on c.391C>T of the RUNX2 gene.
@ast
A new phenotypic variant in cl ...... on c.391C>T of the RUNX2 gene.
@en
type
label
A new phenotypic variant in cl ...... on c.391C>T of the RUNX2 gene.
@ast
A new phenotypic variant in cl ...... on c.391C>T of the RUNX2 gene.
@en
prefLabel
A new phenotypic variant in cl ...... on c.391C>T of the RUNX2 gene.
@ast
A new phenotypic variant in cl ...... on c.391C>T of the RUNX2 gene.
@en
P2860
P50
P356
P1433
P1476
A new phenotypic variant in cl ...... on c.391C>T of the RUNX2 gene.
@en
P2093
Michele Callea
P2860
P356
10.1136/BCR-12-2011-5422
P577
2012-12-05T00:00:00Z