A pericentric inversion of chromosome six in a patient with Peutz-Jeghers' syndrome and the use of FISH to localise the breakpoints on a genetic map.
Karyotypic analysis in a patient with Peutz-Jeghers' syndrome demonstrated a pericentric inversion on chromosome 6. Further investigation was undertaken using fluorescence in situ hybridisation (FISH) with yeast artificial chromosome clones selected to contain genetic markers from chromosome 6,...
المؤلفون الرئيسيون: | Markie, D, Huson, S, Maher, E, Davies, A, Tomlinson, I, Bodmer, W |
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التنسيق: | Journal article |
اللغة: | English |
منشور في: |
1996
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مواد مشابهة
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Peutz-Jeghers syndrome.
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Testing candidate loci on chromosomes 1 and 6 for genetic linkage to Peutz-Jeghers' disease.
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A serine/threonine kinase gene defective in Peutz-Jeghers syndrome.
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Somatic mutations in the Peutz-Jeghers (LKB1/STKII) gene in sporadic malignant melanomas.
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Laugier-Hunziker syndrome: an important differential diagnosis for Peutz-Jeghers syndrome.
حسب: Lampe, A, وآخرون
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