Diagnosis of mutations by the PCR double RFLP method (PCR-dRFLP)

This publication has 11 references indexed in Scilit:

• Identification of a common mutation in the carnitine palmitoyltransferase II gene in familial recurrent myoglobinuria patients
  Nature Genetics, 1993
• Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome
  Human Molecular Genetics, 1993
• Mutagenically separated PCR (MS-PCR): a highly specific one step procedure for easy mutation detection
  Nucleic Acids Research, 1993
• Single base pair mutation analysis by PNA directed PCR clamping
  Nucleic Acids Research, 1993
• K-tuple frequency in the human genome and polymerase chain reaction
  Nucleic Acids Research, 1991
• Genomic DNA sequence of the cystic fibrosis transmembrane conductance regulator (CFTR) gene
  Genomics, 1991
• Diagnosis of genetic disease by primer-specified restriction map modification, with application to cystic fibrosis and retinitis pigmentosa
  The Lancet, 1991
• Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS)
  Nucleic Acids Research, 1989
• Detection of minority point mutations by modified PCR technique: a new approach for a sensitive diagnosis of tumor-progression markers
  Nucleic Acids Research, 1989
• Primer-Directed Enzymatic Amplification of DNA with a Thermostable DNA Polymerase
  Science, 1988