Detecting single base substitutions as heteroduplex polymorphisms

This publication has 14 references indexed in Scilit:

• A deletion of two nucleotides in exon 10 of the CFTR gene in a Soviet family with cystic fibrosis causing early infant death
  Genomics, 1991
• PCR-fingerprinting for selection of HLA matched unrelated marrow donors
  The Lancet, 1991
• Rapid detection of single base mismatches as heteroduplexes on Hydrolink gels
  Trends in Genetics, 1991
• Diagnostic single strand conformational polymorphism, (SSCP): a simplified non-radioisotopic method as applied to a Tay-Sachs B1 variant
  Nucleic Acids Research, 1991
• Population and pedigree studies reveal a lack of association between the dopamine D2 receptor gene and alcoholism
  Published by American Medical Association (AMA) ,1990
• Direct detection and automated sequencing of individual alleles after electrophoretic strand separation: identification of a common nonsense mutation in exon 9 of the human lipoprotein lipase gene
  Nucleic Acids Research, 1990
• A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutations
  Published by Elsevier ,1990
• Multiple mutations in highly conserved residues are found in mildly affected cystic fibrosis patients
  Cell, 1990
• Identification of a factor IX point mutation using SSCP analysis and direct sequencing
  Nucleic Acids Research, 1990
• Detection of Single Base Substitutions by Ribonuclease Cleavage at Mismatches in RNA:DNA Duplexes
  Science, 1985