Citations for
1MYH8, TPCS
Phenotypic variation in trismus-pseudocamptodactyly syndrome caused by a recurrent MYH8 mutation.
Minzer-Conzetti K, Wu E, Vargervik K, Slavotinek A.
Clin Dysmorphol 17(1):1-4. 2008
2FSS, IBM3, MMS, MPD1, MYH2, MYH3, MYH7, MYH8, SHHS, TPCS
Thick filament diseases.
Oldfors A, Lamont PJ.
Adv Exp Med Biol 642:78-91. Review.PMID: 19181095 2008
3MYH8, TPCS
Trismus-pseudocamptodactyly syndrome: case report ten years after.
Gasparini G, Boniello R, Moro A, Zampino G, Pelo S.
Eur J Paediatr Dent 9(4):199-203.PMID: 19072009 2008
4MYH8, TPCS
Trismus-pseudocamptodactyly syndrome is caused by recurrent mutation of MYH8.
Toydemir RM, Chen H, Proud VK, Martin R, van Bokhoven H, Hamel BC, Tuerlings JH, Stratakis CA, Jorde LB, Bamshad MJ.
Am J Med Genet A 140(22):2387-93. 2006
5CNCTP, MYH8, TPCS
Mutation of perinatal myosin heavy chain associated with a Carney complex variant.
Veugelers M, Bressan M, McDermott DA, Weremowicz S, Morton CC, Mabry CC, Lefaivre JF, Zunamon A, Destree A, Chaudron JM, Basson CT.
N Engl J Med 351(5):460-9. 2004
6TPCS
A revised and extended classification of the distal arthrogryposes.
Bamshad M, Jorde LB, Carey JC.
Am J Med Genet 65(4):277-81. Review. 1996