Cleidocranial dysplasia: oral features and genetic analysis of 11 patients-Reference-Cited by-同舟云学术

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Cleidocranial dysplasia: oral features and genetic analysis of 11 patients

Published:2011-10-24 Issue:2 Volume:18 Page:184-190
ISSN:1354-523X
Container-title:Oral Diseases
language:en
Short-container-title:

Author:

Bufalino A,Paranaíba LMR,Gouvêa AF,Gueiros LA,Martelli-Júnior H,Junior JJ,Lopes MA,Graner E,de Almeida OP,Vargas PA,Coletta RD

Publisher

Wiley

Subject

General Dentistry,Otorhinolaryngology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1601-0825.2011.01862.x/fullpdf

Reference27 articles.

1. A simple and cost-effective protocol for DNA isolation from buccal epithelial cells;Aidar;Braz Dent J,2007

2. Cleidocranial dysplasia: molecular genetic analysis and phenotypic-based description of a Middle European patient group;Baumert;Am J Med Genet A,2005

3. Runx2 in normal tissues and cancer cells: a developing story;Blyth;Blood Cells Mol Dis,2010

4. Perspectives on RUNX genes: an update;Cohen;Am J Med Genet A,2009

5. Cleidocranial dysplasia with severe parietal bone dysplasia: C-terminal RUNX2 mutations;Cunningham;Birth Defects Res A Clin Mol Teratol,2006

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2. Cleidocranial dysplasia with hypermobile Ehlers-Danlos syndrome: A case report;Radiology Case Reports;2023-01

3. Identification of a novel missense mutation in non-syndromic familial multiple supernumerary teeth;Archives of Oral Biology;2022-11

4. Application of digital positioning guide plates for the surgical extraction of multiple impacted supernumerary teeth: A case report and review of literature;World Journal of Clinical Cases;2022-09-26

5. BMP Signaling Pathway in Dentin Development and Diseases;Cells;2022-07-16

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