Complex phenotype associated with 17q21.31 microdeletion (2012)
- Authors:
- Autor USP: ROSENBERG, CARLA - IB
- Unidade: IB
- Subjects: GENÉTICA MÉDICA; FENÓTIPOS
- Language: Inglês
- Imprenta:
- Publisher place: São Francisco
- Date published: 2012
- Source:
- Título: Posters: Cytogenetics
- Conference titles: Annual Meeting of the American Society of Human Genetics
-
ABNT
TAYLOR, A. Pic et al. Complex phenotype associated with 17q21.31 microdeletion. 2012, Anais.. São Francisco: Instituto de Biociências, Universidade de São Paulo, 2012. Disponível em: http://www.ashg.org/2012meeting/pdf/38731_poster_complete.pdf. Acesso em: 26 dez. 2025. -
APA
Taylor, A. P., Wawruk, H. D., Rosenberg, C., Krepischi, A. C. V., Safatle, H. P. N., Ferrari, L., & Mazzeu, J. F. (2012). Complex phenotype associated with 17q21.31 microdeletion. In Posters: Cytogenetics. São Francisco: Instituto de Biociências, Universidade de São Paulo. Recuperado de http://www.ashg.org/2012meeting/pdf/38731_poster_complete.pdf -
NLM
Taylor AP, Wawruk HD, Rosenberg C, Krepischi ACV, Safatle HPN, Ferrari L, Mazzeu JF. Complex phenotype associated with 17q21.31 microdeletion [Internet]. Posters: Cytogenetics. 2012 ;[citado 2025 dez. 26 ] Available from: http://www.ashg.org/2012meeting/pdf/38731_poster_complete.pdf -
Vancouver
Taylor AP, Wawruk HD, Rosenberg C, Krepischi ACV, Safatle HPN, Ferrari L, Mazzeu JF. Complex phenotype associated with 17q21.31 microdeletion [Internet]. Posters: Cytogenetics. 2012 ;[citado 2025 dez. 26 ] Available from: http://www.ashg.org/2012meeting/pdf/38731_poster_complete.pdf - Number of rare germline CNVs and TP53 mutation types
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