Source: Clinical genetics. Unidade: FM
Subjects: SEQUENCIAMENTO GENÉTICO, DOENÇAS GENÉTICAS, BRASILEIROS, MUTAÇÃO GENÉTICA, INFERTILIDADE FEMININA
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FRANCA, M. M. et al. Identification of the first homozygous 1-bp deletion in GDF9 gene leading to primary ovarian insufficiency by using targeted massively parallel sequencing. Clinical genetics, v. 93, n. 2, p. 408-411, 2018Tradução . . Disponível em: https://doi.org/10.1111/cge.13156. Acesso em: 16 nov. 2024.APA
Franca, M. M., Funari, M. F. A., Nishi, M. Y., Narcizo, A. M., Domenice, S., Costa, E. M. F., et al. (2018). Identification of the first homozygous 1-bp deletion in GDF9 gene leading to primary ovarian insufficiency by using targeted massively parallel sequencing. Clinical genetics, 93( 2), 408-411. doi:10.1111/cge.13156NLM
Franca MM, Funari MFA, Nishi MY, Narcizo AM, Domenice S, Costa EMF, Lerario AM, Mendonça BB de. Identification of the first homozygous 1-bp deletion in GDF9 gene leading to primary ovarian insufficiency by using targeted massively parallel sequencing [Internet]. Clinical genetics. 2018 ; 93( 2): 408-411.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1111/cge.13156Vancouver
Franca MM, Funari MFA, Nishi MY, Narcizo AM, Domenice S, Costa EMF, Lerario AM, Mendonça BB de. Identification of the first homozygous 1-bp deletion in GDF9 gene leading to primary ovarian insufficiency by using targeted massively parallel sequencing [Internet]. Clinical genetics. 2018 ; 93( 2): 408-411.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1111/cge.13156
