Hasil Pencarian - David E. Godler

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  1. 1
    β-glucuronidase use as a single internal control gene may confound analysis in FMR1 mRNA toxicity studies.

    β-glucuronidase use as a single internal control gene may confound analysis in FMR1 mRNA toxicity studies. oleh Claudine M Kraan, Kim M Cornish, Quang M Bui, Xin Li, Howard R Slater, David E Godler

    Diterbitkan 2018-01-01
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  2. 2
    Defining the 3′Epigenetic Boundary of the <i>FMR1</i> Promoter and Its Loss in Individuals with Fragile X Syndrome

    Defining the 3′Epigenetic Boundary of the <i>FMR1</i> Promoter and Its Loss in Individuals with Fragile X Syndrome oleh David E. Godler, Yoshimi Inaba, Minh Q. Bui, David Francis, Cindy Skinner, Charles E. Schwartz, David J. Amor

    Diterbitkan 2023-06-01
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  3. 3
    Exploring autism symptoms in an Australian cohort of patients with Prader-Willi and Angelman syndromes

    Exploring autism symptoms in an Australian cohort of patients with Prader-Willi and Angelman syndromes oleh Emma K. Baker, David E. Godler, Minh Bui, Chriselle Hickerton, Carolyn Rogers, Mike Field, David J. Amor, Lesley Bretherton

    Diterbitkan 2018-08-01
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  4. 4
    DNA Methylation at Birth Predicts Intellectual Functioning and Autism Features in Children with Fragile X Syndrome

    DNA Methylation at Birth Predicts Intellectual Functioning and Autism Features in Children with Fragile X Syndrome oleh Claudine M Kraan, Emma K Baker, Marta Arpone, Minh Bui, Ling Ling, Dinusha Gamage, Lesley Bretherton, Carolyn Rogers, Michael J Field, Tiffany L Wotton, David Francis, Matt F Hunter, Jonathan Cohen, David J Amor, David E Godler

    Diterbitkan 2020-10-01
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  5. 5
    Significantly Elevated <i>FMR1</i> mRNA and Mosaicism for Methylated Premutation and Full Mutation Alleles in Two Brothers with Autism Features Referred for Fragile X Testing

    Significantly Elevated <i>FMR1</i> mRNA and Mosaicism for Methylated Premutation and Full Mutation Alleles in Two Brothers with Autism Features Referred for Fragile X Testing oleh Michael Field, Tracy Dudding-Byth, Marta Arpone, Emma K. Baker, Solange M. Aliaga, Carolyn Rogers, Chriselle Hickerton, David Francis, Dean G. Phelan, Elizabeth E. Palmer, David J. Amor, Howard Slater, Lesley Bretherton, Ling Ling, David E. Godler

    Diterbitkan 2019-08-01
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  6. 6
    Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome

    Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome oleh Emma K. Baker, Marta Arpone, Solange Aliaga Vera, Lesley Bretherton, Alexandra Ure, Claudine M. Kraan, Minh Bui, Ling Ling, David Francis, Matthew F. Hunter, Justine Elliott, Carolyn Rogers, Michael J. Field, Jonathan Cohen, Lorena Santa Maria, Victor Faundes, Bianca Curotto, Paulina Morales, Cesar Trigo, Isabel Salas, Angelica M. Alliende, David J. Amor, David E. Godler

    Diterbitkan 2019-12-01
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  7. 7
    Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic features

    Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic features oleh Emma K. Baker, Marta Arpone, Solange M. Aliaga, Lesley Bretherton, Claudine M. Kraan, Minh Bui, Howard R. Slater, Ling Ling, David Francis, Matthew F. Hunter, Justine Elliott, Carolyn Rogers, Michael Field, Jonathan Cohen, Kim Cornish, Lorena Santa Maria, Victor Faundes, Bianca Curotto, Paulina Morales, Cesar Trigo, Isabel Salas, Angelica M. Alliende, David J. Amor, David E. Godler

    Diterbitkan 2019-05-01
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