Literature DB >> 20299969

Cleidocranial dysplasia with severe parietal bone dysplasia: a new (p.Val124Serfs) RUNX2 mutation.

Bruno Miguel Cardoso1, Juliette Dupont, Susana Castanhinha, Margarida Ejarque-Albuquerque, Sónia Pereira, Gabriel Miltenberger-Miltenyi, Graça Oliveira.   

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Year:  2010        PMID： 20299969     DOI： 10.1097/MCD.0b013e32833593a1

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN： 0962-8827            Impact factor:   0.816


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  4 in total

1.  A rare presentation of cleidocranial dysplasia.

Authors:  Ilse Broeks; Irma E Veenstra-Knol; Arvid W A Kamps
Journal:  BMJ Case Rep       Date:  2012-08-08

2.  Syringic acid, a phenolic acid, promotes osteoblast differentiation by stimulation of Runx2 expression and targeting of Smad7 by miR-21 in mouse mesenchymal stem cells.

Authors:  B Arumugam; K Balagangadharan; N Selvamurugan
Journal:  J Cell Commun Signal       Date:  2018-01-19       Impact factor: 5.782

Review 3.  Delayed Eruption of Permanent Dentition and Maxillary Contraction in Patients with Cleidocranial Dysplasia: Review and Report of a Family.

Authors:  A Impellizzeri; G Midulla; U Romeo; C La Monaca; E Barbato; G Galluccio
Journal:  Int J Dent       Date:  2018-07-04

4.  A Novel 90-kbp Deletion of RUNX2 Associated with Cleidocranial Dysplasia.

Authors:  Yanli Zhang; Xiaohong Duan
Journal:  Genes (Basel)       Date:  2022-06-23       Impact factor: 4.141
  4 in total

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