ReP USP - Resultado da busca

Trabalho de evento
Duplication of EYA1 causes Branchiootic Syndrome in a Brazilian family (2014)
Mingroni Netto, Regina Celia ; Dantas, V. G. L.; Freitas, E.L.; Moraes, A. M. S. M.; Braga, M. C. C.; Ramos, S. B.; Rosenberg, Carla ; Della-Rosa, V.A.
Source: Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidade: IB
Subjects: PERDA AUDITIVA, MAPEAMENTO GENÉTICO, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MINGRONI NETTO, Regina Celia et al. Duplication of EYA1 causes Branchiootic Syndrome in a Brazilian family. 2014, Anais.. Boston: Instituto de Biociências, Universidade de São Paulo, 2014. Disponível em: http://www.ashg.org/2013meeting/abstracts/fulltext/f130123586.htm. Acesso em: 16 nov. 2024.
APA
Mingroni Netto, R. C., Dantas, V. G. L., Freitas, E. L., Moraes, A. M. S. M., Braga, M. C. C., Ramos, S. B., et al. (2014). Duplication of EYA1 causes Branchiootic Syndrome in a Brazilian family. In Abstracts. Boston: Instituto de Biociências, Universidade de São Paulo. Recuperado de http://www.ashg.org/2013meeting/abstracts/fulltext/f130123586.htm
NLM
Mingroni Netto RC, Dantas VGL, Freitas EL, Moraes AMSM, Braga MCC, Ramos SB, Rosenberg C, Della-Rosa VA. Duplication of EYA1 causes Branchiootic Syndrome in a Brazilian family [Internet]. Abstracts. 2014 ;[citado 2024 nov. 16 ] Available from: http://www.ashg.org/2013meeting/abstracts/fulltext/f130123586.htm
Vancouver
Mingroni Netto RC, Dantas VGL, Freitas EL, Moraes AMSM, Braga MCC, Ramos SB, Rosenberg C, Della-Rosa VA. Duplication of EYA1 causes Branchiootic Syndrome in a Brazilian family [Internet]. Abstracts. 2014 ;[citado 2024 nov. 16 ] Available from: http://www.ashg.org/2013meeting/abstracts/fulltext/f130123586.htm
Trabalho de evento-resumo periodico
Is autosomal dominat nonsyndromic deafness in a Brazilian pedigree linked to DFNA7/DFNM1? (2002)
Lezirovitz, Karina; Braga, M. C. C.; Otto, Paulo A ; Mingroni Netto, Regina Celia
Source: Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidade: IB
Subjects: DEFICIENTE AUDITIVO, DOENÇAS HEREDITÁRIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LEZIROVITZ, Karina et al. Is autosomal dominat nonsyndromic deafness in a Brazilian pedigree linked to DFNA7/DFNM1?. Abstracts. Baltimore: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 16 nov. 2024. , 2002
APA
Lezirovitz, K., Braga, M. C. C., Otto, P. A., & Mingroni Netto, R. C. (2002). Is autosomal dominat nonsyndromic deafness in a Brazilian pedigree linked to DFNA7/DFNM1? Abstracts. Baltimore: Instituto de Biociências, Universidade de São Paulo.
NLM
Lezirovitz K, Braga MCC, Otto PA, Mingroni Netto RC. Is autosomal dominat nonsyndromic deafness in a Brazilian pedigree linked to DFNA7/DFNM1? Abstracts. 2002 ; 71( 4): 440 res.1575.[citado 2024 nov. 16 ]
Vancouver
Lezirovitz K, Braga MCC, Otto PA, Mingroni Netto RC. Is autosomal dominat nonsyndromic deafness in a Brazilian pedigree linked to DFNA7/DFNM1? Abstracts. 2002 ; 71( 4): 440 res.1575.[citado 2024 nov. 16 ]
Trabalho de evento-resumo
Distribution of CGG repeats and FRAXAC1/DXS548 alleles in brazilian populations (1999)
Mingroni Netto, Regina Celia ; Angeli, Claudia Blanes; Auricchio, M T B M; Mesquita, E R L; Guimarães, M N K; Vianna-Morgante, Angela M
Source: Abstracts. Conference titles: International Workshop on 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 et al. Distribution of CGG repeats and FRAXAC1/DXS548 alleles in brazilian populations. 1999, Anais.. Strasbourg: Instituto de Biociências, Universidade de São Paulo, 1999. . Acesso em: 16 nov. 2024.
APA
Mingroni Netto, R. C., Angeli, C. B., Auricchio, M. T. B. M., Mesquita, E. R. L., Guimarães, M. N. K., & Vianna-Morgante, A. M. (1999). Distribution of CGG repeats and FRAXAC1/DXS548 alleles in brazilian populations. In Abstracts. Strasbourg: Instituto de Biociências, Universidade de São Paulo.
NLM
Mingroni Netto RC, Angeli CB, Auricchio MTBM, Mesquita ERL, Guimarães MNK, Vianna-Morgante AM. Distribution of CGG repeats and FRAXAC1/DXS548 alleles in brazilian populations. Abstracts. 1999 ;[citado 2024 nov. 16 ]
Vancouver
Mingroni Netto RC, Angeli CB, Auricchio MTBM, Mesquita ERL, Guimarães MNK, Vianna-Morgante AM. Distribution of CGG repeats and FRAXAC1/DXS548 alleles in brazilian populations. Abstracts. 1999 ;[citado 2024 nov. 16 ]
Trabalho de evento-resumo
X-inactivation in fragile-X carriers (1999)
Vianna-Morgante, Angela M ; Costa, S. S.; Otto, Paulo A ; Mingroni Netto, Regina Celia
Source: Abstracts. Conference titles: International Workshop on 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
VIANNA-MORGANTE, Angela M et al. X-inactivation in fragile-X carriers. 1999, Anais.. Strasbourg: Instituto de Biociências, Universidade de São Paulo, 1999. . Acesso em: 16 nov. 2024.
APA
Vianna-Morgante, A. M., Costa, S. S., Otto, P. A., & Mingroni Netto, R. C. (1999). X-inactivation in fragile-X carriers. In Abstracts. Strasbourg: Instituto de Biociências, Universidade de São Paulo.
NLM
Vianna-Morgante AM, Costa SS, Otto PA, Mingroni Netto RC. X-inactivation in fragile-X carriers. Abstracts. 1999 ;[citado 2024 nov. 16 ]
Vancouver
Vianna-Morgante AM, Costa SS, Otto PA, Mingroni Netto RC. X-inactivation in fragile-X carriers. Abstracts. 1999 ;[citado 2024 nov. 16 ]
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: 16 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. 16 ]
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. 16 ]
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: 16 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. 16 ]
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. 16 ]

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