Auralcephalosyndactyly: a new craniosynostosis syndrome or a variant of the Saethre-Chotzen syndrome?

Author:

Legius E,Fryns J P,Van den Berghe H

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference8 articles.

1. Auralcephalosyndactyly: a new hereditary craniosynostosis syndrome;Kurczynski, T.W.; Casperson, S.M.;J Med Genet,1988

2. Saethre H. Ein BeitragzumTurmschadelproblem. (Pathogenese, Erblichkeit und Symptomatologie). Dtsch Z Nervenheilkd 1931; 117:533-55.

3. Eine eigenartige familiare Entwicklungsstorung. (Akrocephalosyndaktylie, Dysostosis craniofacialis und Hypertelorismus.) Monatsschr Kinderheilkd 1932; 55;Chotzen, R.

4. Temtamy S, McKusick V. In: Bergsma D, ed. The genetics of hand malfornations. New York: Alan R Liss, Birth Defects 1978;XIV(3):328-50.

5. SaethreChotzen syndrome: a broad and variable pattern of skeletal malformations;Friedman, J.M.; Hanson, J.W.; Graham, C.B.; Smith, D.W.;J Pediatr,1977

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4. A novel mutation in the TWIST gene, implicated in Saethre-Chotzen syndrome, is found in the original case of Robinow-Sorauf syndrome;Clinical Genetics;2003-06-06

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