An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidism

Authors

Michael R. Bowl, University of Oxford
Andrew Nesbit, University of Oxford
Brian Harding, University of Oxford
Elaine Levy, University of Oxford
Andrew Jefferson, University of Oxford
Emanuela Volpi, University of Oxford
Karine Rizzoti, National Institute for Medical Research, London
Robin Lovell-Badge, National Institute for Medical Research, London
David Schlessinger, National Institute on Aging, Baltimore
Michael P. Whyte, Washington University School of Medicine in St. Louis
Rajesh V. Thakker, University of Oxford

Journal

The Journal of Clinical Investigation

Publication Date

2005

Volume

115

Issue

10

Inclusive Pages

2822-2831

Document Type

Open Access Publication

DOI

10.1172/JCI24156

Rights and Permissions

Published in Volume 115, Issue 10 (October 1, 2005) J Clin Invest. 2005;115(10):2822–2831. doi:10.1172/JCI24156. Copyright © 2005, American Society for Clinical Investigation

Recommended Citation

Bowl, Michael R.; Nesbit, Andrew; Harding, Brian; Levy, Elaine; Jefferson, Andrew; Volpi, Emanuela; Rizzoti, Karine; Lovell-Badge, Robin; Schlessinger, David; Whyte, Michael P.; and Thakker, Rajesh V., "An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidism." The Journal of Clinical Investigation. 115, 10. 2822-2831. (2005).
https://digitalcommons.wustl.edu/open_access_pubs/1524