TBX6, LHX1 and copy number variations in the complex genetics of Müllerian aplasia (2013)
Sandbacka, Maria; Laivuori, Hannele; Freitas, Érika; Halttunen, Mervi; Jokimaa, Varpu; Morin-Papunen, Laure; Rosenberg, Carla 
; Aittomäki, Kristina
Source: Orphanet Journal of Rare Diseases. Unidade: IB
Subjects: AGENESIA, GENÉTICA, MALFORMAÇÕES
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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: 02 nov. 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:10.1186/1750-1172-8-125NLM
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 nov. 02 ] Available from: https://doi.org/10.1186/1750-1172-8-125Vancouver
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 nov. 02 ] Available from: https://doi.org/10.1186/1750-1172-8-125
