References
- Schmid H. Synchondrosis of the laryngotracheal skeleton and tracheostenosis in the Apert-Crouzon syndrome. Zentralbl Allg Pathol 1971; 114: 326–37
- Shimada H, Misugi K. Anomalies of the tracheal cartilage. Acta Pathol Jpn 1979; 29: 1001–11
- Sano J, Shimada H, Misugi K, Kagyo H. Cloverleaf skull syndrome. Acta Pathol Jpn 1982; 32: 887–900
- Walls TR, Senac MO, Vachon L. Acrocephalospondylosyndactyly—a possible new syndrome: Analysis of the vertebral and intervertebral components. Pediatr Pathol 1990; 10: 117–31
- Devine P, Bhan I, Feingold M, Leonidas JC, Wolpert SM. Completely cartilaginous trachea in a child with Jrouzon syndrome. Am J Dis Child 1984; 138: 40–3
- Stone P, Trevenen CL, Mitchell I, Rudd N. Congenital tracheal stenosis in Pfeiffer syndrome. Clin Genet 1990; 38: 145–8
- Landing BH, Wells TR. Tracheobronchial anomalies in children. Perspect Pediatr Padiol 1973; 1: 1–32
- Kreiborg S, Cohen MM, Jr. Characteristics of the infant Apert skull and its subsequent development. J Craniofac Genet Dev Biol 1990; 10: 399–410
- Cohen MM, Jr. Craniosynostosis: Diagnosis, Evaluation and Management. Raven Press, New York 1986
- Holinger PH, Johnstone KC, Parchet VN, Zimmermann AA. Congenital malformations of the trachea bronchi and lungs. Ann Otol Rhinol Laryngol 1952; 61: 1159–80
- Greene DA. Congenital complete tracheal rings. Arch Otolaryngol 1976; 102: 241–3
- Kreiborg S. Crouzon Syndrome A clinical and roentgencephalometric study. Scand J Plast Reconstr Surg(Suppl) 1981; 18: 1–198
- Peterson-Falzone SJ, Pruzansky S, Parris PJ, Laffer JL. Nasopharyngeal dysmorphology in the syndromes of Apert and Crouzon. Cleft Palate J 1981; 18: 237–50
- Griscom NT, Wohl ME. Dimensions of the growing trachea related to age and gender. Am J Rentgenol 1986; 146: 233–7
- Butz RO, Jr. Length and cross-section growth patterns in the human trachea. Pediatrics 1968; 42: 336–41
- Wailoo MP, Emery JL. Normal growth and development of the trachea. Thorax 1982; 37: 584–7
- Cohen MM, Jr, Kreiborg S. The central nervous system in the Apert syndrome. Am J Med Genet 1990; 35–45
- Weiss L, Reynolds WA, Forman TF, Peterson JA. Craniosynostosis, midfacial hypoplasia, and foot abormalities: An autosomal dominant phenotype in a large Amish kindred. J Pediatr 1976; 88: 963–68
- Kreiborg S, Barr M, Jr, Cohen MM, Jr. The cervical spine in the Apert syndrome. Am J Med Genet 1992; 42, in press