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Artigo de periodico
Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways (2014)
Canton, Ana P. M.; Costa, Sílvia S.; Rodrigues, Tatiane C.; Bertola, Debora R.; Malaquias, Alexsandra C.; Correa, Fernanda A.; Arnhold, Ivo J. P.; Rosenberg, Carla ; Jorge, Alexander A. L.
Source: European Journal of Endocrinology. Unidades: IB, FM
Subjects: GENES, IDADE GESTACIONAL, CRESCIMENTO E DESENVOLVIMENTO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CANTON, Ana P. M. et al. Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways. European Journal of Endocrinology, v. 171, n. 2, p. 253-262, 2014Tradução . . Disponível em: https://doi.org/10.1530/eje-14-0232. Acesso em: 05 nov. 2024.
APA
Canton, A. P. M., Costa, S. S., Rodrigues, T. C., Bertola, D. R., Malaquias, A. C., Correa, F. A., et al. (2014). Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways. European Journal of Endocrinology, 171( 2), 253-262. doi:10.1530/eje-14-0232
NLM
Canton APM, Costa SS, Rodrigues TC, Bertola DR, Malaquias AC, Correa FA, Arnhold IJP, Rosenberg C, Jorge AAL. Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways [Internet]. European Journal of Endocrinology. 2014 ; 171( 2): 253-262.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1530/eje-14-0232
Vancouver
Canton APM, Costa SS, Rodrigues TC, Bertola DR, Malaquias AC, Correa FA, Arnhold IJP, Rosenberg C, Jorge AAL. Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways [Internet]. European Journal of Endocrinology. 2014 ; 171( 2): 253-262.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1530/eje-14-0232
Trabalho de evento-resumo
Simple and non- isotopic pcr - based diagnostic test suitable for population screening of fragil x syndrome among mentally handicapped men (1995)
Haddad, Luciana Amaral ; Mingroni Netto, Regina Celia ; Vianna-Morgante, Angela M ; Pena, S D J
Source: Abstracts. Conference titles: International Workshop on the Fragile X and X-Linked Mental Retardation. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
HADDAD, Luciana Amaral et al. Simple and non- isotopic pcr - based diagnostic test suitable for population screening of fragil x syndrome among mentally handicapped men. 1995, Anais.. Tromso: Instituto de Biociências, Universidade de São Paulo, 1995. . Acesso em: 05 nov. 2024.
APA
Haddad, L. A., Mingroni Netto, R. C., Vianna-Morgante, A. M., & Pena, S. D. J. (1995). Simple and non- isotopic pcr - based diagnostic test suitable for population screening of fragil x syndrome among mentally handicapped men. In Abstracts. Tromso: Instituto de Biociências, Universidade de São Paulo.
NLM
Haddad LA, Mingroni Netto RC, Vianna-Morgante AM, Pena SDJ. Simple and non- isotopic pcr - based diagnostic test suitable for population screening of fragil x syndrome among mentally handicapped men. Abstracts. 1995 ;[citado 2024 nov. 05 ]
Vancouver
Haddad LA, Mingroni Netto RC, Vianna-Morgante AM, Pena SDJ. Simple and non- isotopic pcr - based diagnostic test suitable for population screening of fragil x syndrome among mentally handicapped men. Abstracts. 1995 ;[citado 2024 nov. 05 ]
Trabalho de evento-resumo
Size of cgg repeats of the fmr1 locus in premutated and fully mutated heterozygotes and their offspring: implications for the origin of mosaicism (1995)
Mingroni Netto, Regina Celia ; Haddad, Luciana Amaral ; Vianna-Morgante, Angela M
Source: Abstracts. Conference titles: International Workshop on the Fragile X and X-Linked Mental Retardation. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MINGRONI NETTO, Regina Celia e HADDAD, Luciana Amaral e VIANNA-MORGANTE, Angela M. Size of cgg repeats of the fmr1 locus in premutated and fully mutated heterozygotes and their offspring: implications for the origin of mosaicism. 1995, Anais.. Tromso: Instituto de Biociências, Universidade de São Paulo, 1995. . Acesso em: 05 nov. 2024.
APA
Mingroni Netto, R. C., Haddad, L. A., & Vianna-Morgante, A. M. (1995). Size of cgg repeats of the fmr1 locus in premutated and fully mutated heterozygotes and their offspring: implications for the origin of mosaicism. In Abstracts. Tromso: Instituto de Biociências, Universidade de São Paulo.
NLM
Mingroni Netto RC, Haddad LA, Vianna-Morgante AM. Size of cgg repeats of the fmr1 locus in premutated and fully mutated heterozygotes and their offspring: implications for the origin of mosaicism. Abstracts. 1995 ;[citado 2024 nov. 05 ]
Vancouver
Mingroni Netto RC, Haddad LA, Vianna-Morgante AM. Size of cgg repeats of the fmr1 locus in premutated and fully mutated heterozygotes and their offspring: implications for the origin of mosaicism. Abstracts. 1995 ;[citado 2024 nov. 05 ]

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