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Severe cleidocranial dysplasia and hypophosphatasia in a child with microdeletion of the C-terminal region of RUNX2

✍ Scribed by Areeg H. El-Gharbawy; Joseph N. Peeden Jr.; Ralph S. Lachman; John M. Graham Jr.; Stephen R. Moore; David L. Rimoin


Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
185 KB
Volume
152A
Category
Article
ISSN
1552-4825

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