A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
COSTA, Silvia S. et al. The FMR1 premutation as a cause of premature ovarian failure in Brazilian women. Genetics and Molecular Biology, v. 29, n. 3, p. 423-428, 2006Tradução . . Disponível em: https://doi.org/10.1590/s1415-47572006000300002. Acesso em: 10 nov. 2024.
APA
Costa, S. S., Fonseca, Â. M. da, Bagnoli, V. R., & Vianna-Morgante, A. M. (2006). The FMR1 premutation as a cause of premature ovarian failure in Brazilian women. Genetics and Molecular Biology, 29( 3), 423-428. doi:10.1590/s1415-47572006000300002
NLM
Costa SS, Fonseca ÂM da, Bagnoli VR, Vianna-Morgante AM. The FMR1 premutation as a cause of premature ovarian failure in Brazilian women [Internet]. Genetics and Molecular Biology. 2006 ; 29( 3): 423-428.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1590/s1415-47572006000300002
Vancouver
Costa SS, Fonseca ÂM da, Bagnoli VR, Vianna-Morgante AM. The FMR1 premutation as a cause of premature ovarian failure in Brazilian women [Internet]. Genetics and Molecular Biology. 2006 ; 29( 3): 423-428.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1590/s1415-47572006000300002
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CHEROKI, Carola et al. Report of a del22q11 in a patient with Mayer-Rokitansky-Kuster-Hauser (MRKH) anomaly and exclusion of WNT-4, RAR-gamma, and RXR-alpha as major genes determining MRKH anomaly in a study of 25 affected women. American Journal of Medical Genetics. Part A, v. 140A, n. 12, p. 1339-1342, 2006Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.31254. Acesso em: 10 nov. 2024.
APA
Cheroki, C., Krepischi, A. C. V., Rosenberg, C., Jehee, F. S., Mingroni Netto, R. C., Pavanello Filho, I., et al. (2006). Report of a del22q11 in a patient with Mayer-Rokitansky-Kuster-Hauser (MRKH) anomaly and exclusion of WNT-4, RAR-gamma, and RXR-alpha as major genes determining MRKH anomaly in a study of 25 affected women. American Journal of Medical Genetics. Part A, 140A( 12), 1339-1342. doi:10.1002/ajmg.a.31254
NLM
Cheroki C, Krepischi ACV, Rosenberg C, Jehee FS, Mingroni Netto RC, Pavanello Filho I, Zanforlin Filho S, Kim CA, Bagnoli VR, Mendonça BB, Szuhai K, Otto PA. Report of a del22q11 in a patient with Mayer-Rokitansky-Kuster-Hauser (MRKH) anomaly and exclusion of WNT-4, RAR-gamma, and RXR-alpha as major genes determining MRKH anomaly in a study of 25 affected women [Internet]. American Journal of Medical Genetics. Part A. 2006 ; 140A( 12): 1339-1342.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1002/ajmg.a.31254
Vancouver
Cheroki C, Krepischi ACV, Rosenberg C, Jehee FS, Mingroni Netto RC, Pavanello Filho I, Zanforlin Filho S, Kim CA, Bagnoli VR, Mendonça BB, Szuhai K, Otto PA. Report of a del22q11 in a patient with Mayer-Rokitansky-Kuster-Hauser (MRKH) anomaly and exclusion of WNT-4, RAR-gamma, and RXR-alpha as major genes determining MRKH anomaly in a study of 25 affected women [Internet]. American Journal of Medical Genetics. Part A. 2006 ; 140A( 12): 1339-1342.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1002/ajmg.a.31254