Inability to open the mouth fully: autosomic dominant phenotype with facultative camptodactyly and short stature
Hecht F, Beals RK. Inability to open the mouth fully: autosomic dominant phenotype with facultative camptodactyly and short stature. Birth Defects Original Articles 1969:5(3):96-8.
Linkage analysis with the trismus-pseudocamptodactyly syndrome
May
Robertson RD, Spence MA, Sparkes RS, Neiswanger K, Field LL. Linkage analysis with the trismus-pseudocamptodactyly syndrome. Am J Med Genet 1982 May;12(1):115-20.
Anaesthetic implications of the trismus pseudocamptodactyly (Dutch-Kentucky or Hecht Beals) syndrome
Jan
Vaghadia H, Blackstock D. Anaesthetic implications of the trismus pseudocamptodactyly (Dutch-Kentucky or Hecht Beals) syndrome. Can J Anaesth 1988 Jan;35(1):80-5.
Enlargement of the coronoid process with special reference to the Trismus-pseudocamptodactyly Syndrome
In: Stafleu Tholen (eds)
Van Hoof RF. Enlargement of the coronoid process with special reference to the Trismus-pseudocamptodactyly Syndrome. In: Stafleu Tholen (eds). The Netherlands By Leiden. 1973. pp. 1-120.
Autosomal dominant inheritance of shortening of the flexorprofundus muscle-tendons unit with limitation of jaw excursion
Wilson RV et al. Autosomal dominant inheritance of shortening of the flexorprofundus muscle-tendons unit with limitation of jaw excursion. Birth Defects Original Articles 1969:5(3):99-102.