[A contribution to the clinical picture of acrocephalosyndactylia (Apert's syndrome)].

[Article in German]

Supplemental Content

[Apert's syndrome: a case report]. [J Fr Ophtalmol. 2003]
[Apert's syndrome: a case report].
Doutetien C, Laleye A, Tchabi S, Biaou O, Lawani R, Deguenon J, Darboux R, Gnamey D, Bassabi SK. J Fr Ophtalmol. 2003 Sep; 26(7):738-42.
[Clinico genetic discussion on Apert's syndrome. Apropos of a case]. [Arq Neuropsiquiatr. 1976]
[Clinico genetic discussion on Apert's syndrome. Apropos of a case].
Gonçalves A, Da Silva JB. Arq Neuropsiquiatr. 1976 Sep; 34(3):293-7.
[Apert's syndrome. Clinical and cytogenetic study of a case]. [G Ital Dermatol Minerva Dermat...]
[Apert's syndrome. Clinical and cytogenetic study of a case].
Amerio PL, Massasso J, Sargentini S. G Ital Dermatol Minerva Dermatol. 1969 Oct; 44(10):510-3.
Review [Apert's syndrome]. [Arch Stomatol (Napoli). 1988]
Review [Apert's syndrome].
Gombos F, Serpico R, Angelini L. Arch Stomatol (Napoli). 1988 Nov; 29(5):891-903.
Review A case of Pfeiffer syndrome. [J Korean Med Sci. 2006]
Review A case of Pfeiffer syndrome.
Park MS, Yoo JE, Chung J, Yoon SH. J Korean Med Sci. 2006 Apr; 21(2):374-8.

A family study of craniosynostosis, with probable recognition of a distinct syndrome. [J Med Genet. 1982]
A family study of craniosynostosis, with probable recognition of a distinct syndrome.
Carter CO, Till K, Fraser V, Coffey R. J Med Genet. 1982 Aug; 19(4):280-5.

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