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Manuel Ramos-Kuri

Biographic Data

ID4091295
NAMEManuel Ramos-Kuri
GIVEN NAMESManuel
FAMILY NAMERamos-Kuri
SIGNATURERAMOS-KURI M
AFFILIATIONSUniversidad Panamericana
VERIFIEDNo
TOTAL WORKS2
TOTAL CITATIONS1
AUTHOR COUNT2
EDITOR COUNT0
FIRST PUBLICATION YEAR2005
LATEST PUBLICATION YEAR2006
H-INDEX1
  • FMR1 CGG Repeat Distribution and Linked Microsatellite-SNP Haplotypes in Normal Mexican Mestizo and Indigenous Populations

    Xóchitl Adriana Felix-López, Raúl Argüello-García et al.•ARTICLE•Human Biology•2006•Cited by: 1•References: 5

    The (CGG)n repeat size distribution in the FMR1 gene was studied in healthy individuals: 80 X chromosomes of Mexican Mestizos from Mexico City and 33 X chromosomes of Mexican Amerindians from three indigenous communities (Purepechas, Nahuas, and Tzeltales), along with alleles and haplotypes defined by two microsatellite polymorphic markers (DXS548 and FRAXAC1) and two single nucleotide polymorphisms (FMRA and FMRB). Genetic frequencies of Mestizo…

  • Molecular Demonstration of SLC4A1 Gene Deletion in Two Mexican Patients with Ovalocytosis

    Manuel Ramos-Kuri, Joaquin Carrillo Farga et al.•ARTICLE•Human Biology•2005

    We describe the finding of two Mexican patients with a specific 27-bp deletion in the solute carrier family 4 gene (SLC4A1delta27) (also known as the band 3 gene found on chromosome 17q21-q22), characteristic of Southeast Asian ovalocytosis (SAO). The patients were asymptomatic, and the initial diagnosis was made by microscopic observation of the presence of typical stomatocytic ovalocytes. The gene deletion was confirmed by PCR and DNA sequencin…

  • FMR1 CGG Repeat Distribution and Linked Microsatellite-SNP Haplotypes in Normal Mexican Mestizo and Indigenous Populations

    Xóchitl Adriana Felix-López, Raúl Argüello-García et al.•ARTICLE•Human Biology•2006•Cited by: 1•References: 5

    The (CGG)n repeat size distribution in the FMR1 gene was studied in healthy individuals: 80 X chromosomes of Mexican Mestizos from Mexico City and 33 X chromosomes of Mexican Amerindians from three indigenous communities (Purepechas, Nahuas, and Tzeltales), along with alleles and haplotypes defined by two microsatellite polymorphic markers (DXS548 and FRAXAC1) and two single nucleotide polymorphisms (FMRA and FMRB). Genetic frequencies of Mestizo…

  • Molecular Demonstration of SLC4A1 Gene Deletion in Two Mexican Patients with Ovalocytosis

    Manuel Ramos-Kuri, Joaquin Carrillo Farga et al.•ARTICLE•Human Biology•2005

    We describe the finding of two Mexican patients with a specific 27-bp deletion in the solute carrier family 4 gene (SLC4A1delta27) (also known as the band 3 gene found on chromosome 17q21-q22), characteristic of Southeast Asian ovalocytosis (SAO). The patients were asymptomatic, and the initial diagnosis was made by microscopic observation of the presence of typical stomatocytic ovalocytes. The gene deletion was confirmed by PCR and DNA sequencin…

  • FMR1 CGG Repeat Distribution and Linked Microsatellite-SNP Haplotypes in Normal Mexican Mestizo and Indigenous Populations

    Xóchitl Adriana Felix-López, Raúl Argüello-García et al.•ARTICLE•Human Biology•2006•Cited by: 1•References: 5

    The (CGG)n repeat size distribution in the FMR1 gene was studied in healthy individuals: 80 X chromosomes of Mexican Mestizos from Mexico City and 33 X chromosomes of Mexican Amerindians from three indigenous communities (Purepechas, Nahuas, and Tzeltales), along with alleles and haplotypes defined by two microsatellite polymorphic markers (DXS548 and FRAXAC1) and two single nucleotide polymorphisms (FMRA and FMRB). Genetic frequencies of Mestizo…

Biology (2 works) · Evolutionary biology (2 works) · Gene (2 works) · Genetics (2 works) · Allele (1 works) · Cellular transport and secretion (1 works) · Demography (1 works) · Ecology (1 works) · FMR1 (1 works) · Genetics (1 works)

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