TBX6, LHX1 and copy number variations in the complex genetics of Müllerian aplasia (2013)
- Authors:
- Autor USP: ROSENBERG, CARLA - IB
- Unidade: IB
- DOI: 10.1186/1750-1172-8-125
- Subjects: AGENESIA; GENÉTICA; MALFORMAÇÕES
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Orphanet Journal of Rare Diseases
- ISSN: 1750-1172
- Volume/Número/Paginação/Ano: v. 8, art. 125, p. on-line, 2013
- Este periódico é de acesso aberto
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: gold
- Licença: cc-by
-
ABNT
SANDBACKA, Maria et al. TBX6, LHX1 and copy number variations in the complex genetics of Müllerian aplasia. Orphanet Journal of Rare Diseases, v. 8, p. on-line, 2013Tradução . . Disponível em: https://doi.org/10.1186/1750-1172-8-125. Acesso em: 23 abr. 2024. -
APA
Sandbacka, M., Laivuori, H., Freitas, É., Halttunen, M., Jokimaa, V., Morin-Papunen, L., et al. (2013). TBX6, LHX1 and copy number variations in the complex genetics of Müllerian aplasia. Orphanet Journal of Rare Diseases, 8, on-line. doi:10.1186/1750-1172-8-125 -
NLM
Sandbacka M, Laivuori H, Freitas É, Halttunen M, Jokimaa V, Morin-Papunen L, Rosenberg C, Aittomäki K. TBX6, LHX1 and copy number variations in the complex genetics of Müllerian aplasia [Internet]. Orphanet Journal of Rare Diseases. 2013 ; 8 on-line.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1186/1750-1172-8-125 -
Vancouver
Sandbacka M, Laivuori H, Freitas É, Halttunen M, Jokimaa V, Morin-Papunen L, Rosenberg C, Aittomäki K. TBX6, LHX1 and copy number variations in the complex genetics of Müllerian aplasia [Internet]. Orphanet Journal of Rare Diseases. 2013 ; 8 on-line.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1186/1750-1172-8-125 - Number of rare germline CNVs and TP53 mutation types
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Informações sobre o DOI: 10.1186/1750-1172-8-125 (Fonte: oaDOI API)
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