| 1 | MCIA, MCOP2, VSX2
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| Mutations in the CHX10 gene in non-syndromic microphthalmia/anophthalmia patients from Qatar.
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| Faiyaz-Ul-Haque M, Zaidi SH, Al-Mureikhi MS, Peltekova I, Tsui LC, Teebi AS.
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| Clin Genet 72(2):164-6. No abstract available.
2007
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| 2 | ALX4, PFM1, MNX1, SCRA, VSX1, KTCN1, VSX2, MCIA, SOPT, HESX1, HOXD13, PSDY2, MSX2, PFM2, SIX3, HPE2, DCS, SHOX
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| Homeodomain revisited: a lesson from disease-causing mutations.
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| Chi YI.
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| Hum Genet 116(6):433-44. Epub 2005 Feb 23. 2005
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| 3 | MCIA, VSX2
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| CHX10 mutations cause non-syndromic microphthalmia/anophthalmia in Arab and Jewish kindreds.
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| Bar-Yosef U, Abuelaish I, Harel T, Hendler N, Ofir R, Birk OS.
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| Hum Genet um Genet. 2004 Jul 15 [Epub ahead of print] 2004
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| 4 | AIC, AXR2, CCA, CDG1D, DHOF, DPYD, HPE2, JBTS1, MCIA, MCOPCB2, MKS1, MRXS28, NBCCS2, NS1, OFCD, ONCR, OOD1, OPD2, RBP4, RIEG1, RSTS, TCOF1, WLKWS1, ZEB2
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| Ocular coloboma: a reassessment in the age of molecular neuroscience.
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| Gregory-Evans CY, Williams MJ, Halford S, Gregory-Evans K.
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| J Med Genet 41(12):881-91. 2004
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| 5 | VSX2, MCIA
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| Human microphthalmia associated with mutations in the retinal homeobox gene CHX10.
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| Ferda Percin E, Ploder LA, Yu JJ, Arici K, Horsford DJ, Rutherford A, Bapat B, Cox DW, Duncan AM, Kalnins VI, Kocak-Altintas A, Sowden JC, Traboulsi E, Sarfarazi M, McInnes RR.
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| Nat Genet 25(4):397-401. 2000
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