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AE Shrimpton, BR Braddock, LL Thomson, CK Stein and JJ Hoo Molecular delineation of deletions on 2q37.3 in three cases with an Albright hereditary osteodystrophy-like phenotype Clinical Genetics 66

Version of Record online: 20 OCT 2004 | DOI: 10.1111/j.1399-0004.2004.00363.x

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