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Karen Kirkby

Datos Biográficos

ID4787239
NOMBREKaren Kirkby
NOMBRESKaren
APELLIDOKirkby
FIRMAKIRKBY K
ORCID0000-0002-3576-2641
VERIFICADOSí
TOTAL DE OBRAS1
TOTAL DE CITAS2
OBRAS COMO AUTOR1
OBRAS COMO EDITOR0
PRIMER AÑO DE PUBLICACIÓN2005
AÑO MÁS RECIENTE DE PUBLICACIÓN2005
ÍNDICE H1
  • Haplotype Study of Intermediate-Length Alleles at the Fragile X (FMR1) Gene

    Yvette Curlis, Cuiling Zhang et al.•ARTICLE•Human Biology•2005•Citada por: 2•Referencias: 1

    The CGG repeat within the X-chromosome-linked FMR1 gene, which in hyperexpansion (> 200 copies) results in fragile X syndrome, is highly polymorphic. The mechanism of expansion is not well understood, but CGG repeats called intermediate-length or gray zone alleles (approximately equal 35-60 repeats) are thought to make up the FMR1 alleles showing initial steps in this expansion process. It has been hypothesized that the background haplotype of th…

  • Haplotype Study of Intermediate-Length Alleles at the Fragile X (FMR1) Gene

    Yvette Curlis, Cuiling Zhang et al.•ARTICLE•Human Biology•2005•Citada por: 2•Referencias: 1

    The CGG repeat within the X-chromosome-linked FMR1 gene, which in hyperexpansion (> 200 copies) results in fragile X syndrome, is highly polymorphic. The mechanism of expansion is not well understood, but CGG repeats called intermediate-length or gray zone alleles (approximately equal 35-60 repeats) are thought to make up the FMR1 alleles showing initial steps in this expansion process. It has been hypothesized that the background haplotype of th…

  • Haplotype Study of Intermediate-Length Alleles at the Fragile X (FMR1) Gene

    Yvette Curlis, Cuiling Zhang et al.•ARTICLE•Human Biology•2005•Citada por: 2•Referencias: 1

    The CGG repeat within the X-chromosome-linked FMR1 gene, which in hyperexpansion (> 200 copies) results in fragile X syndrome, is highly polymorphic. The mechanism of expansion is not well understood, but CGG repeats called intermediate-length or gray zone alleles (approximately equal 35-60 repeats) are thought to make up the FMR1 alleles showing initial steps in this expansion process. It has been hypothesized that the background haplotype of th…

Allele (1 obra) · Autism Spectrum Disorder Research (1 obra) · Biology (1 obra) · Epigenetics and DNA Methylation (1 obra) · FMR1 (1 obra) · Gene (1 obra) · Genetics (1 obra) · Genetics (1 obra) · Genetics and Neurodevelopmental Disorders (1 obra) · Haplotype (1 obra)

Ethnos_APP • Proyecto Open Source • Licencia MIT • Frontend v2.0.0 • Privacidad y Cookies • Documentación de la API: api.ethnos.app/docs • Código de la API: GitHub • DOI: 10.5281/zenodo.17049435 • Código del Frontend: GitHub • DOI: 10.5281/zenodo.17050053 • cruz.rio.br • Expectantes Misericordiae