Pitfalls of automated comparative sequence analysis as a single platform for routine clinical testing for NF1

J Med Genet. 2005 May;42(5):e25.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • DNA Mutational Analysis / methods*
  • Genes, Neurofibromatosis 1*
  • Genetic Testing / methods*
  • Humans
  • Mutation
  • Neurofibromatosis 1 / diagnosis*
  • Polymorphism, Genetic
  • Sensitivity and Specificity