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Filtros : "Rosenberg, Carla" "Svartman, Marta" Limpar

Filtros

Artigo de periodico
Subtelomeric 6p25 deletion/duplication: report of a patient with new clinical findings and genotype–phenotype correlations (2015)
Linhares, Natália D; Svartman, Marta; Rodrigues, Tatiane C; Rosenberg, Carla ; Valadares, Eugênia R
Source: European Journal of Medical Genetics. Unidade: IB
Subjects: GENÓTIPOS, FENÓTIPOS, GENOMAS, PROTEÍNAS, GENÉTICA MÉDICA, CITOGENÉTICA MOLECULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LINHARES, Natália D et al. Subtelomeric 6p25 deletion/duplication: report of a patient with new clinical findings and genotype–phenotype correlations. European Journal of Medical Genetics, v. 58, n. 5, p. 310-318, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.ejmg.2015.02.011. Acesso em: 23 jul. 2024.
APA
Linhares, N. D., Svartman, M., Rodrigues, T. C., Rosenberg, C., & Valadares, E. R. (2015). Subtelomeric 6p25 deletion/duplication: report of a patient with new clinical findings and genotype–phenotype correlations. European Journal of Medical Genetics, 58( 5), 310-318. doi:10.1016/j.ejmg.2015.02.011
NLM
Linhares ND, Svartman M, Rodrigues TC, Rosenberg C, Valadares ER. Subtelomeric 6p25 deletion/duplication: report of a patient with new clinical findings and genotype–phenotype correlations [Internet]. European Journal of Medical Genetics. 2015 ; 58( 5): 310-318.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1016/j.ejmg.2015.02.011
Vancouver
Linhares ND, Svartman M, Rodrigues TC, Rosenberg C, Valadares ER. Subtelomeric 6p25 deletion/duplication: report of a patient with new clinical findings and genotype–phenotype correlations [Internet]. European Journal of Medical Genetics. 2015 ; 58( 5): 310-318.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1016/j.ejmg.2015.02.011
Artigo de periodico
Dental developmental abnormalities in a patient with subtelomeric 7q36 deletion syndrome may confirm a novel role for the SHH gene (2014)
Linhares, Natália D.; Svartman, Marta; Salgado, Mauro Ivan; Rodrigues, Tatiane C.; Costa, Sílvia Souza da; Rosenberg, Carla ; Valadares, Eugenia R.
Source: Meta Gene. Unidade: IB
Subjects: ANOMALIA DENTÁRIA, GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LINHARES, Natália D. et al. Dental developmental abnormalities in a patient with subtelomeric 7q36 deletion syndrome may confirm a novel role for the SHH gene. Meta Gene, v. 2, p. 16-24, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.mgene.2013.10.005. Acesso em: 23 jul. 2024.
APA
Linhares, N. D., Svartman, M., Salgado, M. I., Rodrigues, T. C., Costa, S. S. da, Rosenberg, C., & Valadares, E. R. (2014). Dental developmental abnormalities in a patient with subtelomeric 7q36 deletion syndrome may confirm a novel role for the SHH gene. Meta Gene, 2, 16-24. doi:10.1016/j.mgene.2013.10.005
NLM
Linhares ND, Svartman M, Salgado MI, Rodrigues TC, Costa SS da, Rosenberg C, Valadares ER. Dental developmental abnormalities in a patient with subtelomeric 7q36 deletion syndrome may confirm a novel role for the SHH gene [Internet]. Meta Gene. 2014 ; 2 16-24.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1016/j.mgene.2013.10.005
Vancouver
Linhares ND, Svartman M, Salgado MI, Rodrigues TC, Costa SS da, Rosenberg C, Valadares ER. Dental developmental abnormalities in a patient with subtelomeric 7q36 deletion syndrome may confirm a novel role for the SHH gene [Internet]. Meta Gene. 2014 ; 2 16-24.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1016/j.mgene.2013.10.005

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