Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis-Reference-Cited by-同舟云学术

Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis

Published:2013-01-27 Issue:3 Volume:45 Page:304-307
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Sharma Vikram P, ,Fenwick Aimée L,Brockop Mia S,McGowan Simon J,Goos Jacqueline A C,Hoogeboom A Jeannette M,Brady Angela F,Jeelani Nu Owase,Lynch Sally Ann,Mulliken John B,Murray Dylan J,Phipps Julie M,Sweeney Elizabeth,Tomkins Susan E,Wilson Louise C,Bennett Sophia,Cornall Richard J,Broxholme John,Kanapin Alexander,Johnson David,Wall Steven A,van der Spek Peter J,Mathijssen Irene M J,Maxson Robert E,Twigg Stephen R F,Wilkie Andrew O M

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.2531.pdf

Reference26 articles.

1. Lajeunie, E., Le Merrer, M., Bonaïti-Pellie, C., Marchac, D. & Renier, D. Genetic study of nonsyndromic coronal craniosynostosis. Am. J. Med. Genet. 55, 500–504 (1995).

2. Boulet, S.L., Rasmussen, S.A. & Honein, M.A. A population-based study of craniosynostosis in metropolitan Atlanta, 1989–2003. Am. J. Med. Genet. 146A, 984–991 (2008).

3. Wilkie, A.O.M. et al. Prevalence and complications of single-gene and chromosomal disorders in craniosynostosis. Pediatrics 126, e391–e400 (2010).

4. Howard, T.D. et al. Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome. Nat. Genet. 15, 36–41 (1997).

5. El Ghouzzi, V. et al. Mutations of the TWIST gene in the Saethre-Chotzen syndrome. Nat. Genet. 15, 42–46 (1997).

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