Cephalometrical and mutational analyses of familial case of Crouzon syndrome.

MIYAMTO M; MORISHIGE Y; MIYATAKE E; KURATANI T; YAMASHIRO T; TAKANO-YAMAMOTO T

Art

J-GLOBAL ID：200902132770224565 Reference number：02A0132766

Cephalometrical and mutational analyses of familial case of Crouzon syndrome.

Crouzon症候群家族性症例の頭部規格写真分析と変異分析

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Material：
Volume： 60 Issue： 6 Page： 393-397 Publication year： 2001
JST Material Number： F0540A ISSN： 1344-0241 Document type： Article
Article type：原著論文 Country of issue： Japan (JPN) Language： ENGLISH (EN)

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Diagnostics of congenital diseases, deformities. , Biometry , Molecular genetics in general

Reference (19)：

COHEN, M. M. Jr. Crouzon syndrome. Craniosynostosis, Diagnosis, evaluation, and management. 2000, 361-365
KREIBORG, S. Crouzon syndrome, A clinical and roento-gencephalometric study. Scand J Plast Reconstr Surg Suppl. 1981, 18, 1-198
HALL, B. D. Kleeblattschadel (cloverleaf) syndrome : Severe form of Crouzon's syndrome?. J Pediatr. 1972, 80, 526-528
REARDON, W. Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome. Nature Genet. 1994, 8, 98-103
WILKIE, A. O. M. Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome. Nature Genet. 1995, 9, 165-172

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