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Touraine Philippe
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http://hub.abes.fr/oup/periodical/humrep/2007/volume_22/issue_1/101093humrepdel346/authorship/8
http://hub.abes.fr/oup/periodical/hmg/2001/volume_10/issue_15/101093hmg10151591/authorship/16
http://hub.abes.fr/oup/periodical/humrep/2010/volume_25/issue_1/101093humrepdep355/authorship/9
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FOXL2 mutations lead to different ovarian phenotypes in BPES patients: Case Report
Serum anti-Müllerian hormone expression in women with premature ovarian failure
Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype-phenotype correlation
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