New mutations in the CBFA1 gene in two Mexican patients with cleidocranial dysplasia
- 1 May 2002
- journal article
- case report
- Published by Wiley in Clinical Genetics
- Vol. 61 (5), 349-353
- https://doi.org/10.1034/j.1399-0004.2002.610505.x
Abstract
Cleidocranial dysplasia (CCD) is an autosomal dominant skeletal disorder exhibiting a wide clinical spectrum ranging from minimal anomalies to classic CCD. Mutations scattered throughout the entire C...Keywords
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