| 1 | OTX2, SIX1, SIX6
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| Branchiootorenal syndrome and oculoauriculovertebral spectrum features associated with duplication of SIX1, SIX6, and OTX2 resulting from a complex chromosomal rearrangement.
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| Ou Z, Martin DM, Bedoyan JK, Cooper ML, Chinault AC, Stankiewicz P, Cheung SW.
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| Am J Med Genet A 146A(19):2480-9.
2008
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| 2 | SIX3, SIX6, IDH1, CDH18
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| Expression analysis of SIX3 and SIX6 in human tissues reveals differences in expression and a novel correlation between the expression of SIX3 and the genes encoding isocitrate dehyhrogenase and cadherin 18.
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| Aijaz S, Allen J, Tregidgo R, van Heyningen V, Hanson I, Clark BJ.
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| Genomics 86(1):86-99. Epub 2005 Apr 18. 2005
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| 3 | SIX6, BAPA, DEL14Q22
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| Analysis of the developmental SIX6 homeobox gene in patients with anophthalmia/microphthalmia.
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| Gallardo ME, Rodriguez De Cordoba S, Schneider AS, Dwyer MA, Ayuso C, Bovolenta P.
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| Am J Med Genet 129A(1):92-4. No abstract available. 2004
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| 4 | SIX6
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| Tissue-specific regulation of retinal and pituitary precursor cell proliferation.
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| Li X, Perissi V, Liu F, Rose DW, Rosenfeld MG.
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| Science 297(5584):1180-3. 2002
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| 5 | BAPA, SIX6
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| Exclusion of SIX6 hemizygosity in a child with anophthalmia, panhypopituitarism and renal failure.
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| Rauchman M, Hoffman WH, Hanna JD, Kulharya AS, Figueroa RE, Yang J, Tuck-Miller CM.
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| Am J Med Genet 104 : 31-36. 2001
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| 6 | BAPA, SIX2, SIX4, SIX6, DEL14Q22
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| Genomic cloning and characterization of the human homeobox gene SIX6 reveals a cluster of SIX genes in chromosome 14 and associates SIX6 hemizygosity with bilateral anophthalmia and pituitary anomalies.
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| Gallardo ME, Lopez-Rios J, Fernaud-Espinosa I, Granadino B, Sanz R, Ramos C, Ayuso C, Seller MJ, Brunner HG, Bovolenta P, Rodriguez de Cordoba S.
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| Genomics 61(1):82-91. 1999
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