Quantification of GRB10 in 7p12-p14 by fluorogenic 5′ nuclease chemistry and application for genetic diagnosis in Silver-Russell syndrome

This publication has 13 references indexed in Scilit:

• A multiplex methylation PCR assay for identification of uniparental disomy of chromosome 7
  Human Mutation, 2003
• Molecular Genetic Studies of Human Chromosome 7 in Russell–Silver Syndrome
  Genomics, 2002
• Silver-Russell syndrome: a dissection of the genetic aetiology and candidate chromosomal regions
  Journal of Medical Genetics, 2001
• Gene Dosage Analysis in Silver-Russell Syndrome: Use of Quantitative Competitive PCR and Dual-Color FISH to Estimate the Frequency of Duplications in 7p11.2–p13
  Genetic Testing, 2001
• Maternal repression of the human GRB10 gene in the developing central nervous system; evaluation of the role for GRB10 in Silver-Russell syndrome
  European Journal of Human Genetics, 2001
• Conflicting Reports of Imprinting Status of Human GRB10 in Developing Brain: How Reliable Are Somatic Cell Hybrids for Predicting Allelic Origin of Expression?
  American Journal of Human Genetics, 2001
• Diagnosis of haploidy and triploidy based on measurement of gene copy number by real-time PCR
  Human Mutation, 2000
• Human GRB10 is imprinted and expressed from the paternal and maternal allele in a highly tissue- and isoform-specific fashion
  Human Molecular Genetics, 2000
• Duplication of 7p11.2-p13, Including GRB10, in Silver-Russell Syndrome
  American Journal of Human Genetics, 2000
• Growth and symptoms in Silver-Russell syndrome: Review on the basis of 386 patients
  European Journal of Pediatrics, 1995