Molecular delineation of deletions on 2q37.3 in three cases with an Albright hereditary osteodystrophy-like phenotype
Article first published online: 20 OCT 2004
Volume 66, Issue 6, pages 537–544, December 2004
How to Cite
Shrimpton, A., Braddock, B., Thomson, L., Stein, C. and Hoo, J. (2004), Molecular delineation of deletions on 2q37.3 in three cases with an Albright hereditary osteodystrophy-like phenotype. Clinical Genetics, 66: 537–544. doi: 10.1111/j.1399-0004.2004.00363.x
- Issue published online: 1 NOV 2004
- Article first published online: 20 OCT 2004
- Received 15 April 2004, revised and accepted for publication 13 August 2004
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