References

1. Cohen MM Jr. Craniosynostosis: diagnosis, evaluation and management. New York: Raven Press, 1986.

2. Slavkin HC, Bonner JJ. Genetic control mechanisms during early oral facial development. In Stewart RE, Prescott GH, editors. Oral facial clefts. St Louis: CV Mosby, 1976; 1.

3. Higginbottom MC, Jones KL, James HE. Intrauterine constraint and craniosynostosis. Neurosurgery 1980; 6:39.

4. Cohen MM Jr. Craniosynostosis: phenotypic/molecular correlations. Amer J Med Genetics 1995;56:334-9.

5. Marchac D, Renier D. Functional and morphological outcome in 62 Apert's syndrome. Presented at the Fifth International congress of Craniofacial Surgery, October 1993, Oaxaca, Mexico.

6. Atkinson FRB. Hereditary craniofacial dysostosis, or Crouzon's disease. Med Press Circular 1937;195:118-24.

7. Kreiborg S. Crouzon syndrome. Scand J Plast Reconstr Surg 1981;(Suppl 18):1-198.

8. Erickson JD, Cohen MM Jr. A study of parental age effects on the occurrence of fresh mutations for the Apert syndrome. Ann Hum Genet (London) 1974;38: 89-96.

9. Tunte W, Lenz W. Zur Haufigkeit und Mutationstrates des Apert-syndroms. Hum Genet 1967;4:104-11.

10. Blank CE. Apert's syndrome: observations on a British series of thirty-nine cases. Ann Hum Genet 1969;24: 151-64.

11. Cohen MM Jr. An etiologic and nosologic overview of craniosynostosis syndromes. Birth Defects 1975;11(2): 137-89.

12. Lefebvre A. A psychiatric profile before and after reconstructive surgery in children with Apert's syndrome. Br J Plast Surg 1986;39:510-13.

13. Gorlin R, Cohen MM Jr, Levin L. Syndromes with cran-iosynostosis in syndromes of the head and neck. 3rd Edition. New York: Oxford University Press, 1990; 520-1.

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