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| Year | Number of Results |
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| 2001 | 1 |
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Evolution and expression of FOXL2.
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.
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
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The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome.
Crisponi L, Deiana M, Loi A, Chiappe F, Uda M, Amati P, Bisceglia L, Zelante L, Nagaraja R, Porcu S, Ristaldi MS, Marzella R, Rocchi M, Nicolino M, Lienhardt-Roussie A, Nivelon A, Verloes A, Schlessinger D, Gasparini P, Bonneau D, Cao A, Pilia G.
Crisponi L, et al.
Nat Genet. 2001 Feb;27(2):159-66. doi: 10.1038/84781.
Nat Genet. 2001.
PMID: 11175783
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