A case of neonatal osteofibrous dysplasia with novel CDK12 and DDR2 mutations
Author:
Publisher
Elsevier BV
Subject
Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism
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4. Mutations in DDR2 gene cause SMED with short limbs and abnormal calcifications;Bargal;Am. J. Hum. Genet.,2009
5. Osteofibrous dysplasia: a report of two cases;Castellote;Skelet. Radiol.,1988
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