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David Francis

Showing results (131-140 of 176) with videos related to

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Clinical Chemistry|January 12, 2012
Fragile X mental retardation 1 (FMR1) intron 1 methylation in blood predicts verbal cognitive impairment in female carriers of expanded FMR1 alleles: evidence from a pilot studyDavid E Godler, Howard R Slater, Quang M Bui, et al.
Clinical Chemistry|December 31, 2015
Identification of Males with Cryptic Fragile X Alleles by Methylation-Specific Quantitative Melt AnalysisSolange M Aliaga, Howard R Slater, David Francis, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|November 12, 2019
EML1-associated brain overgrowth syndrome with ribbon-like heterotopiaRenske Oegema, George McGillivray, Richard Leventer, et al.
Neuro-Degenerative Diseases|September 8, 2016
Novel Blood Biomarkers Are Associated with White Matter Lesions in Fragile X- Associated Tremor/Ataxia SyndromeDanuta Z Loesch, Sarah J Annesley, Nicholas Trost, et al.
Human Mutation|August 19, 2011
Extending the scope of diagnostic chromosome analysis: detection of single gene defects using high-resolution SNP microarraysDamien L Bruno, Zornitza Stark, David J Amor, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 29, 2011
Evidence for the toxicity of bidirectional transcripts and mitochondrial dysfunction in blood associated with small CGG expansions in the FMR1 gene in patients with parkinsonismDanuta Z Loesch, David E Godler, Andrew Evans, et al.
Nature Plants|September 18, 2023
Redesigning the tomato fruit shape for mechanized productionQiang Zhu, Lei Deng, Jie Chen, et al.
Nature Plants|January 8, 2024
Author Correction: Redesigning the tomato fruit shape for mechanized productionQiang Zhu, Lei Deng, Jie Chen, et al.
International Journal of Molecular Sciences|August 14, 2019
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 TestingMichael Field, Tracy Dudding-Byth, Marta Arpone, et al.
Clinical Genetics|July 10, 2026
Elucidating the Role of SET as a Key Contributor to Neurodevelopmental Disability Within the 9q34.11 Deletion Syndrome IntervalAngelo Condell, Elaine Zhang, Tim Sikora, et al.
Pageof 18

Showing results (131-140 of 176) with videos related to

Sort By:
Pageof 18
Clinical Chemistry|January 12, 2012
Fragile X mental retardation 1 (FMR1) intron 1 methylation in blood predicts verbal cognitive impairment in female carriers of expanded FMR1 alleles: evidence from a pilot studyDavid E Godler, Howard R Slater, Quang M Bui, et al.
Clinical Chemistry|December 31, 2015
Identification of Males with Cryptic Fragile X Alleles by Methylation-Specific Quantitative Melt AnalysisSolange M Aliaga, Howard R Slater, David Francis, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|November 12, 2019
EML1-associated brain overgrowth syndrome with ribbon-like heterotopiaRenske Oegema, George McGillivray, Richard Leventer, et al.
Neuro-Degenerative Diseases|September 8, 2016
Novel Blood Biomarkers Are Associated with White Matter Lesions in Fragile X- Associated Tremor/Ataxia SyndromeDanuta Z Loesch, Sarah J Annesley, Nicholas Trost, et al.
Human Mutation|August 19, 2011
Extending the scope of diagnostic chromosome analysis: detection of single gene defects using high-resolution SNP microarraysDamien L Bruno, Zornitza Stark, David J Amor, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 29, 2011
Evidence for the toxicity of bidirectional transcripts and mitochondrial dysfunction in blood associated with small CGG expansions in the FMR1 gene in patients with parkinsonismDanuta Z Loesch, David E Godler, Andrew Evans, et al.
Nature Plants|September 18, 2023
Redesigning the tomato fruit shape for mechanized productionQiang Zhu, Lei Deng, Jie Chen, et al.
Nature Plants|January 8, 2024
Author Correction: Redesigning the tomato fruit shape for mechanized productionQiang Zhu, Lei Deng, Jie Chen, et al.
International Journal of Molecular Sciences|August 14, 2019
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 TestingMichael Field, Tracy Dudding-Byth, Marta Arpone, et al.
Clinical Genetics|July 10, 2026
Elucidating the Role of SET as a Key Contributor to Neurodevelopmental Disability Within the 9q34.11 Deletion Syndrome IntervalAngelo Condell, Elaine Zhang, Tim Sikora, et al.
Pageof 18