Trismus pseudocamptodactyly syndrome

Author:

Mabry C. Charlton,Barnett Ina S.,Hutcheson M. William,Sorenson Herbert W.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference10 articles.

1. Short muscle syndrome;Mabry;Pediatr. Res.,1973

2. Enlargement of the coronoid process with special reference to the trismus-pseudocamptodactyly syndrome (family studies by Dr. B. G. A. ter Haar);Van Hoof,1973

3. Inability to open the mouth fully; an autosomal dominant phenotype with facultative camptodactyly and short stature (preliminary note);Hecht,1969

4. Autosomal dominant inheritance of shortening of the flexor profundus muscle tendon unit with limitation of jaw excursion;Wilson,1969

5. Shortened flexor tendons in hands and feet associated with limitation of mouth opening (abst. No. 628);Surana,1971

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3. Trismus-Pseudocamptodactyly Syndrome;Atlas of Genetic Diagnosis and Counseling;2017

4. Trismus-Pseudocamptodactyly Syndrome;Atlas of Genetic Diagnosis and Counseling;2016

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