Quantification of PCR Bias Caused by a Single Nucleotide Polymorphism in SMN Gene Dosage Analysis

This publication has 25 references indexed in Scilit:

• Genetic risk assessment in carrier testing for spinal muscular atrophy
  American Journal of Medical Genetics, 2002
• Spinal Muscular Atrophy Genetic Testing Experience at an Academic Medical Center
  The Journal of Molecular Diagnostics, 2002
• Quantitative Analyses of SMN1 and SMN2 Based on Real-Time LightCycler PCR: Fast and Highly Reliable Carrier Testing and Prediction of Severity of Spinal Muscular Atrophy
  American Journal of Human Genetics, 2002
• Heteroduplex Formation in SMN Gene Dosage Analysis
  The Journal of Molecular Diagnostics, 2001
• SMN gene duplication and the emergence of the SMN2 gene occurred in distinct hominids: SMN2 is unique to Homo sapiens
  Human Genetics, 2001
• Quantitative Analysis of Survival Motor Neuron Copies: Identification of Subtle SMN1 Mutations in Patients with Spinal Muscular Atrophy, Genotype-Phenotype Correlation, and Implications for Genetic Counseling
  American Journal of Human Genetics, 1999
• Identification of Proximal Spinal Muscular Atrophy Carriers and Patients by Analysis of SMNT and SMNC Gene Copy Number
  American Journal of Human Genetics, 1997
• Structure and Organization of the Human Survival Motor Neurone (SMN) Gene
  Genomics, 1996
• Identification and characterization of a spinal muscular atrophy-determining gene
  Cell, 1995
• Preferential PCR amplification of alleles: mechanisms and solutions.
  Genome Research, 1992