Fluorescence In Situ Hybridization with Human Chromosome-Specific Libraries

Pinkel, D., Landegent, J., Collins, C., Fuscoe, J., Segraves, R., Lucas, J., & Gray, J. (1988). Fluorescence In Situ Hybridization with Human Chromosome-Specific Libraries: Detection of Trisomy 21 and Translocations of Chromosome 4. Proceedings of the National Academy of Sciences, 9138-9142.

Type

Journal article

Intellectual base

Primary research

Year

1988

Pages

9138-9142

DOI

10.1073/pnas.85.23.9138

DOI registrant

National Academy of Sciences

Link

https://doi.org/10.1073/pnas.85.23.9138

Cited by

1 citation across 1 artifact.

Domain-specific

• Fluorescence In Situ Hybridization
  • In RNA-FISH, probe sets localize transcripts and may support cell-by-cell transcript counting or subcellular distribution analysis.

Verification

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Registry ID ref:8d46651e1039 · see in the full table