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    Fragile X Syndrome

    Fragile X Syndrome: (FXS) is a genetic disorder. Symptoms often include mild to moderate intellectual disability. ... It is typically due to an expansion of the CGG triplet repeat within the Fragile X mental retardation 1 (FMR1) gene on the X chromosome.

    Webinars

    • APR 20, 2022 | 5:30 AM
      Improving Fetal Fraction of EDTA-Gel NIPS Samples Using Gel-Based Size-Selection
      Improving Fetal Fraction of EDTA-Gel NIPS Samples Using Gel-Based...
      Objective : Evaluation of EDTA-gel blood collection tubes from remote locations for NIPS (Non-invasive prenatal testing). Design: Paired comparisons Population: 61 pregnant women from Britis...
      Speaker: Dr François Rousseau, MD, MSc, FRCPC, FCAHS
      Presented at: Genetics Week Virtual Event Series 2022
      3
      JUL 02, 2020 | 1:30 PM
      Molecular Diagnosis of Genetic Diseases using CE in an era of different technologies
      Molecular Diagnosis of Genetic Diseases using CE in an era of...
      Genetic diseases are known occur due to various types of mutations in the human genome. The molecular assays to diagnose these diseases have been developed based on the type of mutation comm...
      Speaker: Ashwin Dalal, MD
      Presented at: APJ Virtual Genetic Solutions Tour 2020
      3
      MAR 27, 2019 | 10:30 AM
      Panel Discussion: The Benefits and Challenges of Cannabis in Pediatric Conditions in Legal States
      Panel Discussion: The Benefits and Challenges of Cannabis in Pediatric...
      In this panel discussion, parents of medically compromised children using cannabis discuss their experiences of what led them to start cannabis therapy, what delivery methods they currently u...
      Speaker: Kenton Crowley, Pharm. D., FAARFM, ABAAHP , Janelle Donovan , Herah Osborne , Dawn Wells
      Presented at: Cannabis Sciences Virtual Event Series 2019
      1
      MAR 28, 2018 | 10:30 AM
      Panel Discussion: Medical Cannabis in Pediatrics
      Panel Discussion: Medical Cannabis in Pediatrics
      In this panel discussion, parents of children using cannabis discuss their experience Herah Osborne: A mother’s story about her journey with her twins having Fragile X syndrome an...
      Speaker: Kenton Crowley, Pharm. D., FAARFM, ABAAHP , Sebastien Cotte , Janie Maedler , Herah Osborne
      Presented at: Cannabis Sciences Virtual Event Series 2018
      3
      OCT 25, 2017 | 6:00 AM
      WEBINAR #3:  Enabling neurological disease research via DNA fragment analysis on the new SeqStudio genetic analyzer
      WEBINAR #3: Enabling neurological disease research via DNA fragment...
      DATE: October 25, 2017TIME: 06:00am PDT, 09:00am EDTThis is the third topic in the webinar series on ‘Sanger Sequencing & Fragment Analysis made easy’.Repetitive DNA...
      Speaker: Gary Latham, PhD
      Sponsored By: Thermo Fisher Scientific
      3
      SEP 10, 2014 | 10:00 AM
      NGS Lessons in Translational Diagnostics
      NGS Lessons in Translational Diagnostics
      In this webinar, we will describe a comprehensive approach for NGS-based marker discovery and the successful migration of these markers to targeted NGS assays using low-quality (FFPE) and low...
      Speaker: Gary Latham Ph.D. and Brian Haynes, Ph.D.
      Sponsored By: Asuragen, Asuragen
      48
      AUG 20, 2014 | 11:30 AM
      More Comprehensive Views of Human Genetic Variation
      More Comprehensive Views of Human Genetic Variation
      High-throughput short-read DNA sequencing has revolutionized our ability to measure genetic variation in the form of single-nucleotide polymorphisms (SNPs) in human genomes. However, ~75% of...
      Speaker: Jonas Korlach, PhD
      Presented at: Genetics and Genomics Virtual Event Series 2014
      8
    APR 20, 2022 | 5:30 AM
    Improving Fetal Fraction of EDTA-Gel NIPS Samples Using Gel-Based Size-Selection
    Improving Fetal Fraction of EDTA-Gel NIPS Samples Using Gel-Based...
    Objective : Evaluation of EDTA-gel blood collection tubes from remote locations for NIPS (Non-invasive prenatal testing). Design: Paired comparisons Population: 61 pregnant women from Britis...
    Speaker: Dr François Rousseau, MD, MSc, FRCPC, FCAHS
    Presented at: Genetics Week Virtual Event Series 2022
    3
    JUL 02, 2020 | 1:30 PM
    Molecular Diagnosis of Genetic Diseases using CE in an era of different technologies
    Molecular Diagnosis of Genetic Diseases using CE in an era of...
    Genetic diseases are known occur due to various types of mutations in the human genome. The molecular assays to diagnose these diseases have been developed based on the type of mutation comm...
    Speaker: Ashwin Dalal, MD
    Presented at: APJ Virtual Genetic Solutions Tour 2020
    3
    MAR 27, 2019 | 10:30 AM
    Panel Discussion: The Benefits and Challenges of Cannabis in Pediatric Conditions in Legal States
    Panel Discussion: The Benefits and Challenges of Cannabis in Pediatric...
    In this panel discussion, parents of medically compromised children using cannabis discuss their experiences of what led them to start cannabis therapy, what delivery methods they currently u...
    Speaker: Kenton Crowley, Pharm. D., FAARFM, ABAAHP , Janelle Donovan , Herah Osborne , Dawn Wells
    Presented at: Cannabis Sciences Virtual Event Series 2019
    1
    MAR 28, 2018 | 10:30 AM
    Panel Discussion: Medical Cannabis in Pediatrics
    Panel Discussion: Medical Cannabis in Pediatrics
    In this panel discussion, parents of children using cannabis discuss their experience Herah Osborne: A mother’s story about her journey with her twins having Fragile X syndrome an...
    Speaker: Kenton Crowley, Pharm. D., FAARFM, ABAAHP , Sebastien Cotte , Janie Maedler , Herah Osborne
    Presented at: Cannabis Sciences Virtual Event Series 2018
    3
    OCT 25, 2017 | 6:00 AM
    WEBINAR #3:  Enabling neurological disease research via DNA fragment analysis on the new SeqStudio genetic analyzer
    WEBINAR #3: Enabling neurological disease research via DNA fragment...
    DATE: October 25, 2017TIME: 06:00am PDT, 09:00am EDTThis is the third topic in the webinar series on ‘Sanger Sequencing & Fragment Analysis made easy’.Repetitive DNA...
    Speaker: Gary Latham, PhD
    Sponsored By: Thermo Fisher Scientific
    3
     
     
  • SEP 10, 2014 | 10:00 AM
    NGS Lessons in Translational Diagnostics
    NGS Lessons in Translational Diagnostics
    In this webinar, we will describe a comprehensive approach for NGS-based marker discovery and the successful migration of these markers to targeted NGS assays using low-quality (FFPE) and low...
    Speaker: Gary Latham Ph.D. and Brian Haynes, Ph.D.
    Sponsored By: Asuragen, Asuragen
    48
    AUG 20, 2014 | 11:30 AM
    More Comprehensive Views of Human Genetic Variation
    More Comprehensive Views of Human Genetic Variation
    High-throughput short-read DNA sequencing has revolutionized our ability to measure genetic variation in the form of single-nucleotide polymorphisms (SNPs) in human genomes. However, ~75% of...
    Speaker: Jonas Korlach, PhD
    Presented at: Genetics and Genomics Virtual Event Series 2014
    8
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