| 1 | MRX45, ZNF81
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| 335.4 kb microduplication in chromosome band Xp11.2p11.3 associated with developmental delay, growth retardation, autistic disorder and dysmorphic features.
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| Alesi V, Bertoli M, Barrano G, Torres B, Pusceddu S, Pastorino M, Perria C, Nardone AM, Novelli A, Serra G.
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| Gene 505(2):384-7. doi: 10.1016/j.gene.2012.05.031. Epub 2012 May 24.
2012
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| 2 | FTSJ1, MRX44, MRX45, ZNF81
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| Microduplication of Xp11.23p11.3 with effects on cognition, behavior, and craniofacial development.
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| El-Hattab AW, Bournat J, Eng PA, Wu JB, Walker BA, Stankiewicz P, Cheung SW, Brown CW.
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| Clin Genet 79(6):531-8. doi: 10.1111/j.1399-0004.2010.01496.x.
2011
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| 3 | ZNF41, ZNF674, ZNF673, MRX50, MRX45, ZNF81, MRX92, MRX89
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| ZNF674: A New Kruppel-Associated Box-Containing Zinc-Finger Gene Involved in Nonsyndromic X-Linked Mental Retardation.
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| Lugtenberg D, Yntema HG, Banning MJ, Oudakker AR, Firth HV, Willatt L, Raynaud M, Kleefstra T, Fryns JP, Ropers HH, Chelly J, Moraine C, Gecz J, Reeuwijk J, Nabuurs SB, de Vries BB, Hamel BC, de Brouwer AP, Bokhoven H.
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| Am J Hum Genet 78(2):265-78. Epub 2005 Dec 29. 2006
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| 4 | MRX45, ZNF81
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| Zinc finger 81 (ZNF81) mutations associated with X-linked mental retardation.
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| Kleefstra T, Yntema HG, Oudakker AR, Banning MJ, Kalscheuer VM, Chelly J, Moraine C, Ropers HH, Fryns JP, Janssen IM, Sistermans EA, Nillesen WN, de Vries LB, Hamel BC, van Bokhoven H.
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| J Med Genet 41(5):394-9. No abstract available. 2004
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| 5 | MRX14, MRX15, MRX21, MRX30, MRX88, MRX54, MRX41, MRX35, MRX44, MRX45, MRX46, MRX48, MRX49, MRX50, MRX51, MRX52, MRX55, MRXS31
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| X-linked nonspecific mental retardation (MRX) linkage studies in 25 unrelated families: the European XLMR consortium.
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| des Portes V, Beldjord C, Chelly J, Hamel B, Kremer H, Smits A, van Bokhoven H, Ropers HH, Claes S, Fryns JP, Ronce N, Gendrot C, Toutain A, Raynaud M, Moraine C.
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| Am J Med Genet 85(3):263-5. No abstract available. 1999
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| 6 | MRX35, MRX44, MRX45, MRX52
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| Four families (MRX43, MRX44, MRX45, MRX52) with nonspecific X-linked mental retardation: clinical and psychometric data and results of linkage analysis.
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| Hamel BC, Smits AP, van den Helm B, Smeets DF, Knoers NV, van Roosmalen T, Thoonen GH, Assman-Hulsmans CF, Ropers HH, Mariman EC, Kremer H.
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| Am J Med Genet 85(3):290-304. 1999
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