| 1 | CDIPT, FOXL2, PFOXIC, POF3
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| Ovarian-specific expression of a new gene regulated by the goat PIS region and transcribed by a FOXL2 bidirectional promoter.
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| Pannetier M, Renault L, Jolivet G, Cotinot C, Pailhoux E.
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| Genomics 85(6):715-26. 2005
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| 2 | FOXL2, BPES, POF3
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| Foxl2 is required for commitment to ovary differentiation.
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| Ottolenghi C, Omari S, Garcia-Ortiz JE, Uda M, Crisponi L, Forabosco A, Pilia G, Schlessinger D.
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| Hum Mol Genet 14(14):2053-62. Epub 2005 Jun 8. 2005
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| 3 | FOXL2, POF3
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| Mutations in the coding region of the FOXL2 gene are not a major cause of idiopathic premature ovarian failure.
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| Bodega B, Porta C, Crosignani PG, Ginelli E, Marozzi A.
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| Mol Hum Reprod 10(8):555-7. Epub 2004 Jun 4. 2004
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| 4 | BPES, FOXL2, POF3
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| FOXL2 and BPES: mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation
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| De Baere E, Beysen D, Oley C, Lorenz B, Cocquet J, De Sutter P, Devriendt K, Dixon M, Fellous M, Fryns JP, Garza A, Jonsrud C, Koivisto PA, Krause A, Leroy BP, Meire F, Plomp A, Van Maldergem L, De Paepe A, Veitia R, Messiaen L.
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| Am J Hum Genet 72(2):478-87. 2003
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| 5 | BPES, FOXL2, POF3
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| A novel mutation in the FOXL2 gene in a patient with blepharophimosis syndrome: differential role of the polyalanine tract in the development of the ovary and the eyelid.
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| Kosaki K, Ogata T, Kosaki R, Sato S, Matsuo N.
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| Ophthalmic Genet 23(1):43-7. 2002
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| 6 | FOXL2, POF3
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| Identification of novel mutations in FOXL2 associated with premature ovarian failure.
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| Harris SE, Chand AL, Winship IM, Gersak K, Aittomaki K, Shelling AN.
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| Mol Hum Reprod 8(8):729-33. 2002
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| 7 | BPES, FOXL2, POF3
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| Mutations in FOXL2 underlying BPES (types 1 and 2) in Colombian families.
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| Ramirez-Castro JL, Pineda-Trujillo N, Valencia AV, Muneton CM, Botero O, Trujillo O, Vasquez G, Mora BE, Durango N, Bedoya G, Ruiz-Linares A.
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| Am J Med Genet 113(1):47-51. 2002
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| 8 | POF1, POF1B, POF3
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| Genes and translocations involved in POF.
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| Schlessinger D, Herrera L, Crisponi L, Mumm S, Percesepe A, Pellegrini M, Pilia G, Forabosco A.
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| Am J Med Genet 111(3):328-33. Review. 2002
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