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Cytogenetic analyses on patients with Crouzon's and Apert's syndromes

✍ Scribed by JOACHIM MARK; JAN LILJA; GÖRAN STENMAN; CLAES LAURITZEN


Book ID
114809182
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
215 KB
Volume
105
Category
Article
ISSN
0018-0661

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A case of Apert's syndrome with posterior (occipital) encephalocele and absence of corpus callosum is described. This is a rare combination. The mechanisms involved are discussed.