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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1964 1
1971 1
1974 1
1976 1
1979 2
1981 1
1983 2
1984 1
1986 2
1987 2
1988 2
1989 2
1990 1
1991 1
1992 1
1993 3
1994 4
1995 6
1996 2
1997 2
1998 2
1999 2
2000 2
2001 6
2002 3
2003 4
2004 2
2005 1
2023 0

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PubMed (OMIM) for id: 66312

60 results

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Page 1
Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndrome.
Beysen D, Raes J, Leroy BP, Lucassen A, Yates JR, Clayton-Smith J, Ilyina H, Brooks SS, Christin-Maitre S, Fellous M, Fryns JP, Kim JR, Lapunzina P, Lemyre E, Meire F, Messiaen LM, Oley C, Splitt M, Thomson J, Van de Peer Y, Veitia RA, De Paepe A, De Baere E. Beysen D, et al. Am J Hum Genet. 2005 Aug;77(2):205-18. doi: 10.1086/432083. Epub 2005 Jun 16. Am J Hum Genet. 2005. PMID: 15962237 Free PMC article.
The human FOXL2 mutation database.
Beysen D, Vandesompele J, Messiaen L, De Paepe A, De Baere E. Beysen D, et al. Hum Mutat. 2004 Sep;24(3):189-93. doi: 10.1002/humu.20079. Hum Mutat. 2004. PMID: 15300845
FOXL2 and BPES: mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation.
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. De Baere E, et al. Am J Hum Genet. 2003 Feb;72(2):478-87. doi: 10.1086/346118. Epub 2003 Jan 14. Am J Hum Genet. 2003. PMID: 12529855 Free PMC article.
Evolution and expression of FOXL2.
Cocquet J, Pailhoux E, Jaubert F, Servel N, Xia X, Pannetier M, De Baere E, Messiaen L, Cotinot C, Fellous M, Veitia RA. Cocquet J, et al. J Med Genet. 2002 Dec;39(12):916-21. doi: 10.1136/jmg.39.12.916. J Med Genet. 2002. PMID: 12471206 Free PMC article. No abstract available.
Mutations in FOXL2 underlying BPES (types 1 and 2) in Colombian families.
Ramírez-Castro JL, Pineda-Trujillo N, Valencia AV, Muñetón CM, Botero O, Trujillo O, Vásquez G, Mora BE, Durango N, Bedoya G, Ruiz-Linares A. Ramírez-Castro JL, et al. Am J Med Genet. 2002 Nov 15;113(1):47-51. doi: 10.1002/ajmg.10741. Am J Med Genet. 2002. PMID: 12400065
60 results