Heterozygotes and homozygotes: discrimination by chemical cleavage of mismatch.

Samankaltaisia teoksia

• Screening for mutations in the phenylalanine hydroxylase gene from Italian patients with phenylketonuria by using the chemical cleavage method: a new splice mutation.
  Tekijä: Dianzani, I, et al.
  Julkaistu: (1991)
• Mutation detection in phenylketonuria by using chemical cleavage of mismatch: importance of using probes from both normal and patient samples.
  Tekijä: Forrest, S M, et al.
  Julkaistu: (1991)
• 35S-labelled probes improve detection of mismatched base pairs by chemical cleavage.
  Tekijä: Saleeba, J A, et al.
  Julkaistu: (1991)
• Longitudinal modeling of frontal cognition in APOE ε4 homozygotes, heterozygotes, and noncarriers
  Tekijä: Caselli, R.J., et al.
  Julkaistu: (2011)
• Leukocyte β-glucosidase in homozygotes and heterozygotes for Gaucher disease
  Tekijä: Raghavan, S. S., et al.
  Julkaistu: (1980)