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,...

وصف كامل

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون: Markie, D, Huson, S, Maher, E, Davies, A, Tomlinson, I, Bodmer, W
التنسيق: Journal article
اللغة:English
منشور في: 1996

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