S. A. Asdell, The genetic sex on intersexual goats and a probable linkage with the gene for hornlessness, Science, vol.99, p.124, 1944.

P. Berta, J. R. Hawkins, A. H. Sinclair, A. Taylor, B. L. Griffiths et al., Genetic evidence equating SRY and the testis-determining factor, Nature, vol.348, pp.448-450, 1990.

J. Cocquet, E. Pailhoux, F. Jaubert, N. Servel, X. Xia et al., Evolution and expression of FOXL2, J. Med. Genet, vol.39, pp.916-921, 2002.
URL : https://hal.archives-ouvertes.fr/hal-02678819

L. Crisponi, M. Deiana, A. Loi, F. Chiappe, M. Uda et al., The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome, Nat. Genet, vol.27, pp.159-166, 2001.

D. Baere, E. Dixon, M. J. Small, K. W. Jabs, E. W. Leroy et al., Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype-phenotype correlation, Hum. Mol. Genet, vol.10, pp.1591-1600, 2001.

P. Koopman, The genetics and biology of vertebrate sex determination, Cell, vol.105, pp.843-847, 2001.

K. A. Loffler, D. Zarkower, and P. Koopman, Etiology of ovarian failure in blepharophimosis ptosis epicanthus inversus syndrome: FOXL2 is a conserved, early-acting gene in vertebrate ovarian development, Endocrinology, vol.144, pp.3237-3243, 2003.

E. Pailhoux, B. Vigier, S. Chaffaux, N. Servel, S. Taourit et al., A 11.7-kb deletion triggers intersexuality and polledness in goats, Nat. Genet, vol.29, pp.453-458, 2001.
URL : https://hal.archives-ouvertes.fr/hal-02674752

E. Pailhoux, B. Vigier, D. Vaiman, N. Servel, S. Chaffaux et al., Ontogenesis of female-to-male sex-reversal in XX polled goats, Dev. Dyn, vol.224, pp.39-50, 2002.
URL : https://hal.archives-ouvertes.fr/hal-02681363

M. Pannetier, N. Servel, J. Cocquet, N. Besnard, C. Cotinot et al., Expression studies of the PIS-regulated genes suggest different mechanisms of sex determination within mammals, Cytogenet. Genome Res, vol.101, pp.199-205, 2003.
URL : https://hal.archives-ouvertes.fr/hal-02675835

L. Schibler, D. Vaiman, A. Oustry, N. Guinec, A. Dangy-caye et al., Construction and extensive characterization of a goat Bacterial Artificial Chromosome library with threefold genome coverage, Mamm. Genome, vol.9, pp.119-124, 1998.
URL : https://hal.archives-ouvertes.fr/hal-02689495

L. Schibler, E. P. Cribiu, A. Oustry-vaiman, J. Furet, and D. Vaiman, Fine mapping suggests that the goat Polled Intersex Syndrome and the human Blepharophimosis Ptosis Epicanthus Syndrome map to a 100-kb homologous region, Genome Res, vol.10, pp.311-318, 2000.
URL : https://hal.archives-ouvertes.fr/hal-02691781

A. Swain, E. Zanaria, A. Hacker, R. Lovell-badge, and G. Camerino, Mouse Dax1 expression is consistent with a role in sex determination as well as in adrenal and hypothalamus function, Nat. Genet, vol.12, pp.404-409, 1996.

D. Vaiman, O. Koutita, A. Oustry, J. Elsen, E. Manfredi et al., Genetic mapping of the autosomal region involved in XX sex-reversal and horn development in goats, Mamm. Genome, vol.7, pp.133-137, 1996.
URL : https://hal.archives-ouvertes.fr/hal-02690403

D. Vaiman, E. Pailhoux, L. Schibler, A. Oustry, S. Chaffaux et al., Genetic mapping of the polled/intersex locus (PIS) in goats, Theriogenology, vol.47, pp.103-109, 1997.
URL : https://hal.archives-ouvertes.fr/hal-02689451

D. Vaiman, L. Schibler, A. Oustry-vaiman, E. Pailhoux, T. Goldammer et al., High-resolution human/goat comparative map of the goat polled/intersex syndrome (PIS): the human homologue is contained in a human YAC from HSA3q23, Genomics, vol.56, pp.31-39, 1999.
URL : https://hal.archives-ouvertes.fr/hal-02691627

S. Vainio, M. Heikkilä, A. Kispert, N. Chin, and A. P. Mcmahon, Female development in mammals is regulated by Wnt-4 signalling, Nature, vol.397, pp.405-409, 1999.