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Induced pluripotent stem cells from homozygous Runx2-deficient mice show poor response to vitamin D during osteoblastic differentiation
Online Contents | 2022|Keywords: Cleidocranial dysplasia -
Molecular Genetics of Cleidocranial Dysplasia
Taylor & Francis Verlag | 2021|Keywords: Cleidocranial dysplasia -
Effect and Possible Mechanism of Network Between MicroRNAs and RUNX2 Gene on Human Dental Follicle Cells
Wiley | 2014|Keywords: CLEIDOCRANIAL DYSPLASIA -
Association of polyalanine and polyglutamine coiled coils mediates expansion disease-related protein aggregation and dysfunction.
Free accessBASE | 2014|Keywords: cleidocranial dysplasia -
Cleidocranial dysplasia and RUNX2‐clinical phenotype–genotype correlation
Wiley | 2016|Keywords: Cleidocranial dysplasia -
Skeletal and molecular findings in 51 Cleidocranial dysplasia patients from Turkey
Wiley | 2021|Keywords: Cleidocranial dysplasia -
A novel Alu-mediated microdeletion in the RUNX2 gene in a Chinese patient with cleidocranial dysplasia
Online Contents | 2018|Keywords: cleidocranial dysplasia -
Cleidocranial dysplasia: oral features and genetic analysis of 11 patients
Wiley | 2012|Keywords: cleidocranial dysplasia -
Cleidocranial dysplasia—A case report of incidentally found and lately diagnosed disorder
Free accessWiley | 2022|Keywords: cleidocranial dysplasia -
Familial cleidocranial dysplasia misdiagnosed as rickets over three generations
Wiley | 2015|Keywords: cleidocranial dysplasia -
Clinical spectrum of cleidocranial dysplasia in a family with twins
Wiley | 2013|Keywords: cleidocranial dysplasia -
RUNX2 mutations in cleidocranial dysplasia patients
Wiley | 2010|Keywords: Cleidocranial dysplasia -
Identification of a novel RUNX2 gene mutation and early diagnosis of CCD in a cleidocranial dysplasia suspected Iranian family
Free accessWiley | 2020|Keywords: cleidocranial dysplasia -
Clinical‐radiological approach for the diagnosis of cleidocranial dysplasia in adults: A familial cases series
Free accessWiley | 2021|Keywords: cleidocranial dysplasia -
A novel single‐base deletion of the RUNX Family Transcription Factor 2 gene associated with cleidocranial dysplasia
Wiley | 2023|Keywords: cleidocranial dysplasia -
Novel Mutation of the RUNX2 Gene in Patients with Cleidocranial Dysplasia
Karger Verlag | 2017|Keywords: Cleidocranial dysplasia -
Novel complex disease allele mutations in cleidocranial dysplasia patients
Wiley | 2014|Keywords: cleidocranial dysplasia -
Surgical treatment of multiple impacted supernumerary teeth in a cleidocranial dysplasia patient
Wiley | 2022|Keywords: cleidocranial dysplasia -
Correlation between genotype and supernumerary tooth formation in cleidocranial dysplasia
Wiley | 2010|Keywords: cleidocranial dysplasia -
Identification of a stop codon mutation in the CBFA1 runt domain from a patient with cleidocranial dysplasia and cleft lip
Wiley | 2001|Keywords: cleidocranial dysplasia
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