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Clinical spectrum of cleidocranial dysplasia in a family with twins

  • Published:2013-06 Issue:3 Volume:55 Page:392-395
  • ISSN:1328-8067
  • Container-title:Pediatrics International
  • language:en
  • Short-container-title:Pediatr Int

Author:

Wang Jiangping1,Huang Xinwen2,Lai Can3,Jiang Kewen4

Affiliation:

1. Department of Rehabilitation; Zhejiang University School of Medicine; Hangzhou; China

2. Department of Child Health Care; Zhejiang University School of Medicine; Hangzhou; China

3. Department of Radiology; Zhejiang University School of Medicine; Hangzhou; China

4. Department of Neurology; Children's Hospital; Zhejiang University School of Medicine; Hangzhou; China

Publisher

Wiley

Subject

Pediatrics, Perinatology, and Child Health

Reference11 articles.

1. Mutations in the RUNX2 gene in patients with cleidocranial dysplasia;Otto;Hum. Mutat.,2002

2. RUNX genes, neoplasia, and cleidocranial dysplasia;Cohen;Am. J. Med. Genet.,2001

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

4. Cleidocranial dysplasia: Etiology and stomatognathic and craniofacial abnormalities;D'Alessandro;Minerva Stomatol.,2010

5. Cleidocranial dysplasia: Clinical and molecular genetics;Mundlos;J. Med. Genet.,1999

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