Number of cgg repeats of the fmr1 locus in premutated and fully mutated heterozygotes and their offspring: implications for the origin of mosaicism (1996)
- Authors:
- USP affiliated authors: MORGANTE, ANGELA MARIA VIANNA - IB ; MINGRONI NETTO, REGINA CELIA - IB
- Unidade: IB
- Assunto: GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: American Journal of Medical Genetics
- Volume/Número/Paginação/Ano: v.64, n.2 , p.270-3, aug. 1996
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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: 19 set. 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 set. 19 ] -
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 set. 19 ] - 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
- Genetic diversity of FMR1 CGC and linked microsatellites in South American populations
- Novel fragile site at xq28
- AGG interspersion patterns in the CGG repeat of the FMR1 gene and linked DXS548/FRAXAC1 haplotypes in Brazilian populations
- Distribution of CGG repeats and GRAXAC1/DXS548 alleles in south american populations
- Increased frequency of gray zone-premutated fraxa alleles in brazilian mentally impaired boys
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