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Artigo de periodico
Fully mutated and Gray-zone FRAXA alleles in brazilian mentally retarded boys (1999)
Haddad, Luciana Amaral ; Mingroni Netto, Regina Celia ; Vianna-Morgante, Angela M ; Aguiar, Marcos J B; Costa, Sílvia S; Pena, Sérgio D J
Source: American Journal of Medical Genetics. 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. Fully mutated and Gray-zone FRAXA alleles in brazilian mentally retarded boys. American Journal of Medical Genetics, v. 84, n. 3, p. 198-201, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19990528)84:3%3C198::aid-ajmg5%3E3.0.co;2-w. Acesso em: 16 nov. 2024.
APA
Haddad, L. A., Mingroni Netto, R. C., Vianna-Morgante, A. M., Aguiar, M. J. B., Costa, S. S., & Pena, S. D. J. (1999). Fully mutated and Gray-zone FRAXA alleles in brazilian mentally retarded boys. American Journal of Medical Genetics, 84( 3), 198-201. doi:10.1002/(sici)1096-8628(19990528)84:3%3C198::aid-ajmg5%3E3.0.co;2-w
NLM
Haddad LA, Mingroni Netto RC, Vianna-Morgante AM, Aguiar MJB, Costa SS, Pena SDJ. Fully mutated and Gray-zone FRAXA alleles in brazilian mentally retarded boys [Internet]. American Journal of Medical Genetics. 1999 ; 84( 3): 198-201.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990528)84:3%3C198::aid-ajmg5%3E3.0.co;2-w
Vancouver
Haddad LA, Mingroni Netto RC, Vianna-Morgante AM, Aguiar MJB, Costa SS, Pena SDJ. Fully mutated and Gray-zone FRAXA alleles in brazilian mentally retarded boys [Internet]. American Journal of Medical Genetics. 1999 ; 84( 3): 198-201.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990528)84:3%3C198::aid-ajmg5%3E3.0.co;2-w
Trabalho de evento-resumo
Increased frequency of gray zone-premutated fraxa alleles in brazilian mentally impaired boys (1997)
Haddad, Luciana Amaral ; Aguiar, M J B; Costa, S. S.; Mingroni Netto, Regina Celia ; Vianna-Morgante, Angela M ; Pena, Sérgio D. J.
Source: Abstract. Conference titles: International Workshop on the Fragile X and X-linked Mental Retardation. Unidade: IB
Subjects: RETARDO MENTAL, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
HADDAD, Luciana Amaral et al. Increased frequency of gray zone-premutated fraxa alleles in brazilian mentally impaired boys. 1997, Anais.. Canadá: Instituto de Biociências, Universidade de São Paulo, 1997. . Acesso em: 16 nov. 2024.
APA
Haddad, L. A., Aguiar, M. J. B., Costa, S. S., Mingroni Netto, R. C., Vianna-Morgante, A. M., & Pena, S. D. J. (1997). Increased frequency of gray zone-premutated fraxa alleles in brazilian mentally impaired boys. In Abstract. Canadá: Instituto de Biociências, Universidade de São Paulo.
NLM
Haddad LA, Aguiar MJB, Costa SS, Mingroni Netto RC, Vianna-Morgante AM, Pena SDJ. Increased frequency of gray zone-premutated fraxa alleles in brazilian mentally impaired boys. Abstract. 1997 ;[citado 2024 nov. 16 ]
Vancouver
Haddad LA, Aguiar MJB, Costa SS, Mingroni Netto RC, Vianna-Morgante AM, Pena SDJ. Increased frequency of gray zone-premutated fraxa alleles in brazilian mentally impaired boys. Abstract. 1997 ;[citado 2024 nov. 16 ]
Artigo de periodico
Pcr-based test suitable for screening for fragile x syndrome among mentally retarded males (1996)
Haddad, Luciana Amaral ; Mingroni Netto, Regina Celia ; Vianna-Morgante, Angela M ; Pena, S D J
Source: Human Genetics. 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. Pcr-based test suitable for screening for fragile x syndrome among mentally retarded males. Human Genetics, v. 97, p. 808-12, 1996Tradução . . Disponível em: https://doi.org/10.1007/s004390050141. Acesso em: 16 nov. 2024.
APA
Haddad, L. A., Mingroni Netto, R. C., Vianna-Morgante, A. M., & Pena, S. D. J. (1996). Pcr-based test suitable for screening for fragile x syndrome among mentally retarded males. Human Genetics, 97, 808-12. doi:10.1007/s004390050141
NLM
Haddad LA, Mingroni Netto RC, Vianna-Morgante AM, Pena SDJ. Pcr-based test suitable for screening for fragile x syndrome among mentally retarded males [Internet]. Human Genetics. 1996 ;97 808-12.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1007/s004390050141
Vancouver
Haddad LA, Mingroni Netto RC, Vianna-Morgante AM, Pena SDJ. Pcr-based test suitable for screening for fragile x syndrome among mentally retarded males [Internet]. Human Genetics. 1996 ;97 808-12.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1007/s004390050141
Artigo de periodico
Number of cgg repeats of the fmr1 locus in premutated and fully mutated heterozygotes and their offspring: implications for the origin of mosaicism (1996)
Mingroni Netto, Regina Celia ; Haddad, Luciana Amaral ; Vianna-Morgante, Angela M
Source: American Journal of Medical Genetics. 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. Number of cgg repeats of the fmr1 locus in premutated and fully mutated heterozygotes and their offspring: implications for the origin of mosaicism. American Journal of Medical Genetics, v. 64, n. 2 , p. 270-3, 1996Tradução . . Acesso em: 16 nov. 2024.
APA
Mingroni Netto, R. C., Haddad, L. A., & Vianna-Morgante, A. M. (1996). Number of cgg repeats of the fmr1 locus in premutated and fully mutated heterozygotes and their offspring: implications for the origin of mosaicism. American Journal of Medical Genetics, 64( 2 ), 270-3.
NLM
Mingroni Netto RC, Haddad LA, Vianna-Morgante AM. Number of cgg repeats of the fmr1 locus in premutated and fully mutated heterozygotes and their offspring: implications for the origin of mosaicism. American Journal of Medical Genetics. 1996 ;64( 2 ): 270-3.[citado 2024 nov. 16 ]
Vancouver
Mingroni Netto RC, Haddad LA, Vianna-Morgante AM. Number of cgg repeats of the fmr1 locus in premutated and fully mutated heterozygotes and their offspring: implications for the origin of mosaicism. American Journal of Medical Genetics. 1996 ;64( 2 ): 270-3.[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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