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Article

Pallister‐killian syndrome: Characterization of the isochromosome 12p by fluorescent <i>In Situ</i> hybridization

1 Dec 1991

Abstract excerpt

The isochromosome 12p (i(12p)) in fibroblasts of 3 patients with Pallister-Killian syndrome and one decreased prematurely born neonate, was characterized by fluorescent in situ hybridization (FISH) using chromosome 12-specific DNA probes. FISH is a useful technique for rapid and reliable detection and characterization of the i(12p) chromosome in Pallister-Killian patients. Detection was possible also in...

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PMID: 1789295
DOI: 10.1002/ajmg.1320410321

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Source receipt: pubmed, retrieved 7 Sept 2026.

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Pallister‐killian syndrome: Characterization of the isochromosome 12p by fluorescent <i>In Situ</i> hybridizationPMID 1789295Read ↗

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