Early Detection of Fragile X Syndrome: Applications of a Novel Approach for Improved Quantitative Methylation Analysis in Venous Blood and Newborn Blood Spots

Update: 2014-10-13

Description

Fragile X Syndrome is a severe neurodevelopmental disorder which is both complex and heterogeneous in both clinical phenotype and epigenotype. It is also one of the major inherited conditions co-morbid with autistic behaviors.

Comments

In Channel

Extreme PCR: Efficient and Specific DNA Amplification in 15-60 Seconds

2015-01-1218:22

Refinement of Variant Selection for the LDL Cholesterol Genetic Risk Score in the Diagnosis

2015-01-1209:29

Total and Cause Specific Mortality by Moderately and Markedly Increased Ferritin Concentrations

2015-01-0709:29

Critical Issues in International Biobanking

2014-12-2908:56

Integrative Bioinformatics Analysis Reveals New Prognostic Biomarkers of Clear Cell Renal Cell Carcinoma

2014-12-2308:56

Clinical Genomics: When Whole Genome Sequencing Is like a Wholebody CT Scan

2014-12-1514:34

December Audio Summary

2014-12-0108:26

Emory: Experience with Ebola Patients

2014-11-1308:43

Point/Counterpoint: The Quest for Clean Competition in Sports

2014-11-0408:43

Microfluidic Genotyping by Rapid Serial PCR and High-Speed Melting Analysis

2014-11-0408:43

November 2014 Audio Summary

2014-11-0407:05

Generation of a New Cystatin C–Based Estimating Equation for Glomerular Filtration Rate by Use of 7 Assays Standardized to the International Calibrator

2014-10-2808:57

Where Are All the New Omics-Based Tests?

2014-10-2107:55

Early Detection of Fragile X Syndrome: Applications of a Novel Approach for Improved Quantitative Methylation Analysis in Venous Blood and Newborn Blood Spots

2014-10-1320:45

From Lost in Translation to Paradise Found: Enabling Protein Biomarker Method Transfer by Mass Spectrometry

2014-10-0720:45

Three of 7 Hemoglobin A1c Point-of-Care Instruments Do Not Meet Generally Accepted Analytical Performance Criteria

2014-09-3012:58

Influence of the Confounding Factors Age and Sex on MicroRNA Profiles from Peripheral Blood

2014-09-2206:12

Podcasts Go Platinum!

2014-09-1607:04

Maternal Plasma RNA Sequencing for Genome-Wide Transcriptomic Profiling and Identification of Pregnancy-Associated Transcripts

2014-09-1608:38

September 2014 Audio Summary

2014-09-0406:55

00:00

Early Detection of Fragile X Syndrome: Applications of a Novel Approach for Improved Quantitative Methylation Analysis in Venous Blood and Newborn Blood Spots

#box-pro-ellipsis-176090567943871{-webkit-line-clamp:2;}Early Detection of Fragile X Syndrome: Applications of a Novel Approach for Improved Quantitative Methylation Analysis in Venous Blood and Newborn Blood Spots

Early Detection of Fragile X Syndrome: Applications of a Novel Approach for Improved Quantitative Methylation Analysis in Venous Blood and Newborn Blood Spots

Godler, David

Early Detection of Fragile X Syndrome: Applications of a Novel Approach for Improved Quantitative Methylation Analysis in Venous Blood and Newborn Blood Spots