Source: Fertility and sterility. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, MULHERES, HIPOGONADISMO, OVÁRIO
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CORRÊA, Frederico José Silva et al. A new FOXL2 gene mutation in a woman with premature ovarian failure and sporatic blepharophimosis-ptosis-epicanthus inversus syndrome. Fertility and sterility, n. 3, p. 1006.e3-1006.e6, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.fertnstert.2009.08.034. Acesso em: 11 jun. 2024.APA
Corrêa, F. J. S., Tavares, A. B., Pereira, R. W., & Abrão, M. S. (2010). A new FOXL2 gene mutation in a woman with premature ovarian failure and sporatic blepharophimosis-ptosis-epicanthus inversus syndrome. Fertility and sterility, ( 3), 1006.e3-1006.e6. doi:10.1016/j.fertnstert.2009.08.034NLM
Corrêa FJS, Tavares AB, Pereira RW, Abrão MS. A new FOXL2 gene mutation in a woman with premature ovarian failure and sporatic blepharophimosis-ptosis-epicanthus inversus syndrome [Internet]. Fertility and sterility. 2010 ;( 3): 1006.e3-1006.e6.[citado 2024 jun. 11 ] Available from: https://doi.org/10.1016/j.fertnstert.2009.08.034Vancouver
Corrêa FJS, Tavares AB, Pereira RW, Abrão MS. A new FOXL2 gene mutation in a woman with premature ovarian failure and sporatic blepharophimosis-ptosis-epicanthus inversus syndrome [Internet]. Fertility and sterility. 2010 ;( 3): 1006.e3-1006.e6.[citado 2024 jun. 11 ] Available from: https://doi.org/10.1016/j.fertnstert.2009.08.034
