RUNX2 mutations in Chinese patients with cleidocranial dysplasia.
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Genetic background of supernumerary teethThe cleidocranial dysplasia-related R131G mutation in the Runt-related transcription factor RUNX2 disrupts binding to DNA but not CBF-beta.Novel mutation of RUNX2 gene in a patient with cleidocranial dysplasiaCleidocranial dysplasia: a rare cause of disproportionate severe short statureNovel RUNX2 frameshift mutations in Chinese patients with cleidocranial dysplasia.
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RUNX2 mutations in Chinese patients with cleidocranial dysplasia.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 10 June 2009
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
RUNX2 mutations in Chinese patients with cleidocranial dysplasia.
@en
RUNX2 mutations in Chinese patients with cleidocranial dysplasia.
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type
label
RUNX2 mutations in Chinese patients with cleidocranial dysplasia.
@en
RUNX2 mutations in Chinese patients with cleidocranial dysplasia.
@nl
prefLabel
RUNX2 mutations in Chinese patients with cleidocranial dysplasia.
@en
RUNX2 mutations in Chinese patients with cleidocranial dysplasia.
@nl
P2093
P2860
P356
P1433
P1476
RUNX2 mutations in Chinese patients with cleidocranial dysplasia
@en
P2093
Honghao Zhou
L Darryl Quarles
Wanfeng Xu
Xuewu Chen
P2860
P304
P356
10.1093/MUTAGE/GEP025
P577
2009-06-10T00:00:00Z