Mutations in the human Delta homologue, DLL3, cause axial skeletal defects in spondylocostal dysostosis-Reference-Cited by-同舟云学术

Mutations in the human Delta homologue, DLL3, cause axial skeletal defects in spondylocostal dysostosis

Published:2000-04 Issue:4 Volume:24 Page:438-441
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Bulman Michael P.,Kusumi Kenro,Frayling Timothy M.,McKeown Carole,Garrett Christine,Lander Eric S.,Krumlauf Robb,Hattersley Andrew T.,Ellard Sian,Turnpenny Peter D.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0400_438.pdf

Reference30 articles.

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2. Turnpenny, P.D. et al. A gene for autosomal recessive spondylocostal dysostosis maps to 19q13.1–q13.3. Am. J. Hum. Genet. 65, 175–182 (1999).

3. Kusumi, K. et al. The mouse pudgy mutation disrupts Delta homologue Dll3 and initiation of early somite boundaries. Nature Genet. 19, 274–278 (1998).

4. Conlon, R.A., Reaume, A.G. & Rossant, J. Notch1 is required for the coordinate segmentation of somites. Development 121, 1533–1545 (1995).

5. de Angelis, M.H., McIntyre, J.I. & Gossler, A. Maintenance of somite borders in mice requires the Delta homologue Dll1. Nature 386, 717–721 (1997).

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