Identification of the first homozygous 1-bp deletion in GDF9 gene leading to primary ovarian insufficiency by using targeted massively parallel sequencing (2018)
- Authors:
- Autor USP: MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidade: FM
- DOI: 10.1111/cge.13156
- Subjects: SEQUENCIAMENTO GENÉTICO; DOENÇAS GENÉTICAS; BRASILEIROS; MUTAÇÃO GENÉTICA; INFERTILIDADE FEMININA
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Clinical genetics
- ISSN: 0009-9163
- Volume/Número/Paginação/Ano: v. 93, n. 2, p. 408-411, 2018
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: green
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ABNT
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: 02 jun. 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.13156 -
NLM
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 jun. 02 ] Available from: https://doi.org/10.1111/cge.13156 -
Vancouver
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 jun. 02 ] Available from: https://doi.org/10.1111/cge.13156 - Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absense of SRY sequence in gonadal tissue
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Informações sobre o DOI: 10.1111/cge.13156 (Fonte: oaDOI API)
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