| 1 | PSDY2, PSDY3, PSDY4
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| Synpolydactyly: clinical and molecular advances.
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| Malik S, Grzeschik KH.
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| Clin Genet 73(2):113-20. Epub 2007 Dec 19. Review. 2008
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| 2 | FBLN1, PSDY3, RASSF8
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| The fibulin-1 gene (FBLN1) is disrupted in a t(12;22) associated with a complex type of synpolydactyly.
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| Debeer P, Schoenmakers EF, Twal WO, Argraves WS, De Smet L, Fryns JP, Van De Ven WJ.
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| J Med Genet 39(2):98-104. 2002
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| 3 | PSDY3
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| Physical map of a 1.5 mb region on 12p11.2 harbouring a synpolydactyly associated chromosomal breakpoint.
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| Debeer P, Schoenmakers EF, Thoelen R, Holvoet M, Kuittinen T, Fabry G, Fryns JP, Goodman FR, Van de Ven WJ.
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| Eur J Hum Genet 8(8):561-70. 2000
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| 4 | FBLN1, PSDY3
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| Physical mapping of the t(12;22) translocation breakpoints in a family with a complex type of 3/3'/4 synpolydactyly.
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| Debeer P, Schoenmakers EF, Thoelen R, Fryns JP, Van de Ven WJ.
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| Cytogenet Cell Genet 81(3-4):229-34. 1998
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