Mutational analysis of RUNX2 gene in Chinese patients with cleidocranial dysplasia.
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(+info )Tissue-specific calibration of extracellular matrix material properties by transforming growth factor-beta and Runx2 in bone is required for hearing.
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(+info )Nell-1, a key functional mediator of Runx2, partially rescues calvarial defects in Runx2(+/-) mice.
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(+info )Identification of a novel RUNX2 gene mutation in an Italian family with cleidocranial dysplasia.
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(+info )Cleidocranial dysplasia: a case report.
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(+info )Molecular genetics of supernumerary tooth formation.
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(+info )Advantages of cone beam computed tomography (CBCT) in the orthodontic treatment planning of cleidocranial dysplasia patients: a case report.
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(+info )Characterization of complex chromosomal rearrangements by targeted capture and next-generation sequencing.
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