Literature DB >> 11083386

A stop codon mutation in the CBFA 1 gene causes cleidocranial dysplasia.

F J Tsai1, J Y Wu, W D Lin, C H Tsai.   

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Year:  2000        PMID： 11083386     DOI： 10.1080/080352500750027673

Source DB:  PubMed          Journal:  Acta Paediatr        ISSN： 0803-5253            Impact factor:   2.299


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  3 in total

1.  [Anomalies of the skull in cleidocranial dysplasia].

Authors:  I Golan; A Waldeck; U Baumert; J Strutz; D Müssig
Journal:  HNO       Date:  2004-12       Impact factor: 1.284

2.  Novel mutation of RUNX2 gene in a patient with cleidocranial dysplasia.

Authors:  Ya-Wun Guo; Chih-Yang Chiu; Chien-Lin Liu; Tjin-Shing Jap; Liang-Yu Lin
Journal:  Int J Clin Exp Pathol       Date:  2015-01-01

3.  RUNX2 mutations in Taiwanese patients with cleidocranial dysplasia.

Authors:  Wei-De Lin; Shuan-Pei Lin; Chung-Hsing Wang; Yushin Tsai; Chih-Ping Chen; Fuu-Jen Tsai
Journal:  Genet Mol Biol       Date:  2011-04-01       Impact factor: 1.771
  3 in total

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