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Jeanette J A Holden

Datos Biográficos

ID4091162
NOMBREJeanette J A Holden
NOMBRESJeanette J A
APELLIDOHolden
FIRMAHOLDEN J J A
AFILIACIONESQueen's University
VERIFICADONo
TOTAL DE OBRAS3
TOTAL DE CITAS6
TOTAL COMO AUTOR3
TOTAL COMO EDITOR0
PRIMER AÑO DE PUBLICACIÓN2005
AÑO MÁS RECIENTE DE PUBLICACIÓN2009
ÍNDICE H2
  • Age at Diagnosis of Autism Spectrum Disorders in Four Regions of Canada

    Open Access•Hélène Ouellette‐Kuntz, Hélène M J Ouellette-Kuntz et al.•ARTICLE•Canadian Journal of Public Health•2009•Citada por: 4•Referencias: 17

  • Addressing Health Disparities Through Promoting Equity for Individuals with Intellectual Disability

    Open Access•Hélène Ouellette‐Kuntz, Hélène Ouellette-Kuntz et al.•ARTICLE•Canadian Journal of Public Health•2005•Referencias: 82

  • 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…

  • Age at Diagnosis of Autism Spectrum Disorders in Four Regions of Canada

    Open Access•Hélène Ouellette‐Kuntz, Hélène M J Ouellette-Kuntz et al.•ARTICLE•Canadian Journal of Public Health•2009•Citada por: 4•Referencias: 17

  • 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…

  • Addressing Health Disparities Through Promoting Equity for Individuals with Intellectual Disability

    Open Access•Hélène Ouellette‐Kuntz, Hélène Ouellette-Kuntz et al.•ARTICLE•Canadian Journal of Public Health•2005•Referencias: 82

  • 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…

  • Age at Diagnosis of Autism Spectrum Disorders in Four Regions of Canada

    Open Access•Hélène Ouellette‐Kuntz, Hélène M J Ouellette-Kuntz et al.•ARTICLE•Canadian Journal of Public Health•2009•Citada por: 4•Referencias: 17

Autism Spectrum Disorder Research (2 obras) · Environmental health (2 obras) · Family and Disability Support Research (2 obras) · Genetics and Neurodevelopmental Disorders (2 obras) · Medicine (2 obras) · Population (2 obras) · Psychiatry (2 obras) · Allele (1 obras) · Autism (1 obras) · Autism spectrum disorder (1 obras)

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