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BioMed Research International
Volume 2018, Article ID 1573871, 9 pages
https://doi.org/10.1155/2018/1573871
Review Article

Zone of Polarizing Activity Regulatory Sequence Mutations/Duplications with Preaxial Polydactyly and Longitudinal Preaxial Ray Deficiency in the Phenotype: A Review of Human Cases, Animal Models, and Insights Regarding the Pathogenesis

King Saud University, Riyadh, Saudi Arabia

Correspondence should be addressed to Mohammad M. Al-Qattan; moc.liamtoh@nattaqom

Received 9 October 2017; Revised 19 December 2017; Accepted 16 January 2018; Published 13 February 2018

Academic Editor: Thomas Lufkin

Copyright © 2018 Mohammad M. Al-Qattan. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

How to Cite this Article

Mohammad M. Al-Qattan, “Zone of Polarizing Activity Regulatory Sequence Mutations/Duplications with Preaxial Polydactyly and Longitudinal Preaxial Ray Deficiency in the Phenotype: A Review of Human Cases, Animal Models, and Insights Regarding the Pathogenesis,” BioMed Research International, vol. 2018, Article ID 1573871, 9 pages, 2018. https://doi.org/10.1155/2018/1573871.