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Somatic development in cleidocranial dysplasia

✍ Scribed by Jensen, Birgit Leth


Book ID
102701766
Publisher
John Wiley and Sons
Year
1990
Tongue
English
Weight
502 KB
Volume
35
Category
Article
ISSN
0148-7299

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Cleidocranial dysplasia (CCD) is an autosomal dominant disease characterized by hypoplasia or aplasia of clavicles, open fontanelles, and other skeletal anomalies. A mouse mutant, shown by clinical and radiographic analysis to be strikingly similar to the human disorder and designated Ccd, was used