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Citation: Ha. Phillips et al., CHRNB2 is the second acetylcholine receptor subunit associated with autosomal dominant nocturnal frontal lobe epilepsy, AM J HU GEN, 68(1), 2001, pp. 225-231
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Citation: J. Gecz et al., Characterization of the human glutamate receptor subunit 3 gene (GRIA3), acandidate for bipolar disorder and nonspecific X-linked mental retardation, GENOMICS, 62(3), 1999, pp. 356-368
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Citation: J. Gecz et al., Fibroblast growth factor homologous factor 2 (FHF2): gene structure, expression and mapping to the Borjeson-Forssman-Lehmann syndrome region in Xq26 delineated by a duplication breakpoint in a BFLS-like patient, HUM GENET, 104(1), 1999, pp. 56-63
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Citation: Ak. Gedeon et al., Gene localization for oral-facial-digital syndrome type 1 (OFD1 : MIM 311200) proximal to DXS85, AM J MED G, 82(4), 1999, pp. 352-354
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Citation: Ie. Scheffer et al., Familial partial epilepsy with variable foci: A new partial epilepsy syndrome with suggestion of linkage to chromosome 2, ANN NEUROL, 44(6), 1998, pp. 890-899