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The 18 pages that link to Fluorescence in situ hybridization, each with the reason it gives.

• ChromosomeRelated: This method locates targeted chromosome sequences and rearrangements.

• AneuploidyRelated: It can count targeted chromosome copies in suspected aneuploid cells.

• CytogeneticsRelated: FISH can test a targeted chromosomal region when banding alone lacks resolution.

• 22q11.2 deletion syndromeRelated: Targeted probes can detect common 22q11.2 deletions, though not every atypical deletion.

• DiGeorge syndromeRelated: It can detect the common 22q11.2 deletion, though some smaller or atypical deletions may be missed.

• Molecular pathologyRelated: It shows whether specific genes are amplified, deleted, or rearranged in their tissue context.

• Burkitt lymphomaRelated: It can identify the MYC rearrangement that supports the diagnosis.

• Cri du chat syndromeRelated: A probe targeting 5p can help detect deletions too small to see on a standard karyotype.

• Ewing sarcomaRelated: It can reveal rearrangements involving EWSR1 in tumor samples.

• Chromosome abnormalityRelated: It can test for targeted chromosome gains, losses, or rearrangements.