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References
Cohen MM Pfeiffer syndrome: update, clinical subtypes and guidelines for differential diagnosis Am J Med Genet 1993 43 300–7
Naski MC, Ornitz DM FGF signaling in skeletal development Pediatr Pathol Mol Med 1999 18 355–79
Reardon W, Smith A, Honour JW, et al Evidence for digenic inheritance in some cases of Antley-Bixler syndrome J Med Genet 2000 37 26–32
Kito H, Nogami H, Oki T, Arao K, Nagasaka M, Tanaka Y Antley-Bixler syndrome: a disorder characterized by congenital synostosis of the elbow joint and the cranial suture J Pediatr Orthop 1996 16 243–6
Cohen MM, MacLean RE Craniosynostosis: Diagnosis, Evaluation And Management. 2nd ed Oxford, NY: Oxford University Press 2000 p. 357
Soekarman D, Fryns JP, vanden Berghe H Pfeiffer acrocephalosyndactyly syndrome in mother and son with cloverleaf skull anomaly in the child Genet Couns 1992 3 217–20
Noetzel MJ, Marsh JL, Palkes H, Gado M Hydrocephalus and mental retardation in craniosynostosis J Pediatr 1985 107 885–92
Noorily MR, Farmer DL, Belenky WMN, Philppart AI Congenital tracheal anomalies in the craniosynostosis syndrome J Pediatr Surg 1999 34 1036–39
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Herman, T., Siegel, M. Pfeiffer Syndrome, Type II. J Perinatol 21, 565–567 (2001). https://doi.org/10.1038/sj.jp.7210568
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DOI: https://doi.org/10.1038/sj.jp.7210568