Literature DB >> 10980549

A novel CBFA1 mutation (R190W) in an Italian family with cleidocranial dysplasia.

A Giannotti1, A Tessa, C Patrono, L D Florio, M Velardo, C Dionisi-Vici, E Bertini, F M Santorelli.   

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Year:  2000        PMID： 10980549     DOI： 10.1002/1098-1004(200009)16:3<277::AID-HUMU25>3.0.CO;2-V

Source DB:  PubMed          Journal:  Hum Mutat        ISSN： 1059-7794            Impact factor:   4.878


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  2 in total

1.  The role of periodontal ligament cells in delayed tooth eruption in patients with cleidocranial dysostosis.

Authors:  Stefan Lossdörfer; Bassel Abou Jamra; Birgit Rath-Deschner; Werner Götz; Rami Abou Jamra; Bert Braumann; Andreas Jäger
Journal:  J Orofac Orthop       Date:  2009-12-04       Impact factor: 1.938

2.  A novel small deletion mutation in RUNX2 gene in one Chinese family with cleidocranial dysplasia.

Authors:  Ting Chen; Jin Hou; Ling-Ling Hu; Jie Gao; Bu-Ling Wu
Journal:  Int J Clin Exp Pathol       Date:  2014-04-15
  2 in total

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