Breakpoint characterization of large deletions in EXT1 or EXT2 in 10 multiple osteochondromas families.

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Published in BMC Med Genet on June 26, 2011

Authors

Ivy Jennes1, Danielle de Jong, Kirsten Mees, Pancras C W Hogendoorn, Karoly Szuhai, Wim Wuyts

Author Affiliations

1: Department of Medical Genetics, University and University Hospital of Antwerp, 2650 Edegem, Belgium.

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