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Essays in Biochemistry|November 8, 2019
DNA methylation analysis for screening and diagnostic testing in neurodevelopmental disordersDavid E Godler, David J AmorGenes|September 28, 2021
Special Issue: Genetics of Prader-Willi SyndromeDavid E Godler, Merlin G ButlerGenes|June 28, 2023
Editorial for the Fragile X Syndrome Genetics Special Issue: May 2023David E Godler, William T BrownCurrent Opinion in Psychiatry|January 13, 2025
Genetics of Prader-Willi and Angelman syndromes: 2024 updateDavid E Godler, Deepan Singh, Merlin G ButlerDevelopmental Medicine and Child Neurology|August 8, 2018
Epigenetics of fragile X syndrome and fragile X-related disordersClaudine M Kraan, David E Godler, David J AmorDisability and Health Journal|January 13, 2023
Estimating the impact of Angelman syndrome on parental productivity in Australia using productivity-adjusted life yearsSally L Sansom, Emma K Baker, David E Godler, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 8, 2026
Extended newborn screening using DNA methylation testing for fragile X syndrome in 17,107 infantsDavid E Godler, Ling Ling, Dinusha Gamage, et al.Molecular Genetics & Genomic Medicine|February 23, 2019
Analysis of the Prader-Willi syndrome imprinting center using droplet digital PCR and next-generation whole-exome sequencingSamantha N Hartin, Waheeda A Hossain, David Francis, et al.Journal of Medical Genetics|July 29, 2021
Men with FMR1 premutation alleles of less than 71 CGG repeats have low risk of being affected with fragile X-associated tremor/ataxia syndrome (FXTAS)Ellenore M Martin, Ying Zhu, Claudine M Kraan, et al.Genes|June 2, 2021
Detection of Cryptic Fragile X Full Mutation Alleles by Southern Blot in a Female and Her Foetal DNA via Chorionic Villus Sampling, Complicated by Mosaicism for 45,X0/46,XX/47,XXXAlison Pandelache, David Francis, Ralph Oertel, et al.Pageof 5