| 1 | MYH8, TPCS
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| Phenotypic variation in trismus-pseudocamptodactyly syndrome caused by a recurrent MYH8 mutation.
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| Minzer-Conzetti K, Wu E, Vargervik K, Slavotinek A.
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| Clin Dysmorphol 17(1):1-4. 2008
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| 2 | FSS, IBM3, MMS, MPD1, MYH2, MYH3, MYH7, MYH8, SHHS, TPCS
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| Thick filament diseases.
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| Oldfors A, Lamont PJ.
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| Adv Exp Med Biol 642:78-91. Review.PMID: 19181095 2008
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| 3 | MYH8, TPCS
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| Trismus-pseudocamptodactyly syndrome: case report ten years after.
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| Gasparini G, Boniello R, Moro A, Zampino G, Pelo S.
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| Eur J Paediatr Dent 9(4):199-203.PMID: 19072009 2008
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| 4 | MYH2, MYH3, MYH7, MYH8
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| Hereditary myosin myopathies.
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| Oldfors A.
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| Neuromuscul Disord 17(5):355-67. Epub 2007 Apr 16. Review.PMID: 17434305 2007
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| 5 | MYH8, TPCS
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| Trismus-pseudocamptodactyly syndrome is caused by recurrent mutation of MYH8.
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| Toydemir RM, Chen H, Proud VK, Martin R, van Bokhoven H, Hamel BC, Tuerlings JH, Stratakis CA, Jorde LB, Bamshad MJ.
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| Am J Med Genet A 140(22):2387-93. 2006
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| 6 | CNCTP, MYH8, TPCS
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| Mutation of perinatal myosin heavy chain associated with a Carney complex variant.
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| Veugelers M, Bressan M, McDermott DA, Weremowicz S, Morton CC, Mabry CC, Lefaivre JF, Zunamon A, Destree A, Chaudron JM, Basson CT.
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| N Engl J Med 351(5):460-9. 2004
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| 7 | MYH1, MYH2, MYH3, MYH4, MYH8, MYH13
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| Organization of human and mouse skeletal myosin heavy chain gene clusters is highly conserved.
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| Weiss A, et al.
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| Proc Natl Acad Sci U S A 96(6):2958-2963. 1999
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| 8 | MYH8
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| Characterization of a human perinatal myosin heavy-chain transcript.
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| Jullian EH, Kelly AM, Pompidou AJ, Hoffman R, Schiaffino S, Stedman HH, Rubinstein NA.
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| Eur J Biochem 230(3):1001-6.PMID: 7601129 1995
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| 9 | MYH1, MYH2, MYH3, MYH4, MYH8, MYH10, MYH13
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| Organization of the human skeletal myosin heavy chain gene cluster.
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| Yoon SJ, et al.
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| Proc Natl Acad Sci U S A 89 : 12078-12082. 1992
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| 10 | MYH8
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| Generation of a full-length human perinatal myosin heavy-chain-encoding cDNA.
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| Karsch-Mizrachi I, et al.
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| Gene 89 : 289-294. 1990
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