Increased frequency of gray zone-premutated fraxa alleles in brazilian mentally impaired boys (1997)
- Authors:
- USP affiliated authors: MINGRONI NETTO, REGINA CELIA - IB ; MORGANTE, ANGELA MARIA VIANNA - IB
- Unidade: IB
- Subjects: RETARDO MENTAL; GENÉTICA
- Language: Inglês
- Imprenta:
- Source:
- Título: Abstract
- Conference titles: International Workshop on the Fragile X and X-linked Mental Retardation
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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: 17 out. 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 out. 17 ] -
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 out. 17 ] - Number of cgg repeats of the fmr1 locus in premutated and fully mutated heterozygotes and their offspring: implications for the origin of mosaicism
- DXS548/FRAXAC1 haplotypes in fragile X chromosomes in Brazilian population
- Simple and non- isotopic pcr - based diagnostic test suitable for population screening of fragil x syndrome among mentally handicapped men
- A menopausa precoce é uma manifestação da pré-mutação da síndrome do cromossomo X frágil
- Distribuição das repetições CGG do loco FMR-1 e dos alelos dos microssatélites FRAXAC1/DXS548 em populações brasileiras
- Distribution of CGG repeats and FRAXAC1/DXS548 alleles in brazilian populations
- Distribution of CGG repeats and GRAXAC1/DXS548 alleles in south american populations
- Origin of fmr-1 mutation: study of closely linked microsatellite loci in fragile x syndrome
- Dinâmica das repetições CGG do loco da Síndrome de Cromossomo X Frágil e dos haplótipos associados em populações de diferentes grupos étnicos
- Genetic diversity of FMR1 CGC and linked microsatellites in South American populations
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