Disruption of the C7orf2/Lmbr1 genic region is associated with preaxial polydactyly in humans and mice

2003-12-01

Additional Metadata
Keywords	C7orf2, Lmbr1, Preaxial polydactyly, Ssq, Translocation
Persistent URL	doi.org/10.1007/s007740300000, hdl.handle.net/1765/59701
Journal	Journal of Bone and Mineral Metabolism
Organisation	Department of Clinical Genetics
Citation APA APA Style APA-ALL Style AAA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style American-Institute-of-Physics Style Council-of-Science-Editors Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format	Horikoshi, T., Endo, F., Shibata, M., Heutink, P., Hill, R.& Noji, S. (2003). Disruption of the C7orf2/Lmbr1 genic region is associated with preaxial polydactyly in humans and mice. In Journal of Bone and Mineral Metabolism (Vol. 21, Number 1, pp. 1–4).https://doi.org/10.1007/s007740300000

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