| 1 | EFHC2, TS
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| Identification of EFHC2 as a quantitative trait locus for fear recognition in Turner syndrome.
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| Weiss LA, Purcell S, Waggoner S, Lawrence K, Spektor D, Daly MJ, Sklar P, Skuse D.
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| Hum Mol Genet 16(1):107-13. Epub 2006 Dec 12. 2007
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| 2 | DELXP11, EFHC2, MAOA, MAOB, ND, NDP
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| Contiguous deletion of the NDP, MAOA, MAOB, and EFHC2 genes in a patient with Norrie disease, severe psychomotor retardation and myoclonic epilepsy.
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| Rodriguez-Revenga L, Madrigal I, Alkhalidi LS, Armengol L, González E, Badenas C, Estivill X, Milŕ M.
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| Am J Med Genet A 143A(9):916-20.PMID: 17431911 2007
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| 3 | EFHC2
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| A new EF-hand containing gene EFHC2 on Xp11.4: tentative evidence for association with juvenile myoclonic epilepsy.
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| Gu W, Sander T, Heils A, Lenzen KP, Steinlein OK.
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| Epilepsy Res 66(1-3):91-8. 2005
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