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 | 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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5 | 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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6 | TPCS
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| A revised and extended classification of the distal arthrogryposes.
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| Bamshad M, Jorde LB, Carey JC.
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| Am J Med Genet 65(4):277-81. Review. 1996
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