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Parmi ces anomalies, laquelle (lesquelles) peut (peuvent) être visible(s) en FISH métaphasique ?Une délétion hétérozygote interstitielle 9q32q33 de 2 Mb. Une trisomie 16 en mosaïque de 50%.Une triploïdie homogène.Une translocation réciproque équilibrée t(9;15) avec des fragments échangés de 15 et 35 Mb.Une mutation faux-sens du gène CFTR.

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