Vanek J., Janda J., Amblerova V., Losan F.: Freeman Sheldon syndrome: A disorder of myopathic origin?J Med Genet1986;23: 2,231-236.
3.
Dallapicola B., Giannotti A., Lembo A., Sagui L.: Autosomal recessive form of whistling face syndrome in sibs. Am J Med Genet1989;33:542-544.
4.
Gorlin RJ, Cohen MM, Levin LS: Syndromes of the Head and Neck, 3rd ed. New York, Oxford University Press, 1990.
5.
Antley RM, Uga N., Burzynski NJ, et al: Diagnostic criteria for the "whistling face syndrome." Birth Defects1975;2:161-168.
6.
Marasovich WA , Mazaheri M., Stool SE: Otolaryngologic findings in whistling face syndrome. Arch Otolaryngol Head Neck Surg1989;115:1373-1380.
7.
Galliani CA, Matt BH: Laryngomalacia and intra-neural striated muscle in an infant with the Freeman-Sheldon syndrome. Int J Pediatr OtorhinoLaryngoL1993 ;25:243-248.
8.
Di Rocco M., Errin MI, Lignana E.: Distal arthrogryposis, mental retardation, whistling face and Pierre-Robin sequence: Another case. Am J Med Genet1992 ;44:391.
9.
Hageman G., Willemse J., van Ketel BA, Verdonck Afmm: The pathogenesis of fetal hypokinesia. A neurological study of 75 cases of congenital contractures with emphasis on cerebral lesions. Neuropediatrics1987;18:22-33.
10.
Rao SS, Chary R., Karan S.: Freeman Sheldon syndrome in a newborn (whistling face): A case report . Indian Paediatr1979; 16:291-292.
11.
Illum N., Reske-Nielsen E., Skovby F., et al: Lethal autosomal recessive arthrogryposis multiplex congenita with whistling face and calcifications of the nervous system. Neuropediatrics1988;19:186-192.