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Constitutional t(16;21)(p13;q22) as a novel pathogenomic mechanism in a series of three new RUNX1 mutated FPD/AML pedigrees: implications for diagnostics

Translated title of the contribution: Constitutional t(16;21)(p13;q22) as a novel pathogenomic mechanism in a series of three new RUNX1 mutated FPD/AML pedigrees: implications for diagnostics

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Translated title of the contributionConstitutional t(16;21)(p13;q22) as a novel pathogenomic mechanism in a series of three new RUNX1 mutated FPD/AML pedigrees: implications for diagnostics
Original languageUndefined/Unknown
JournalChromosome Research
Volume19
Publication statusPublished - 2 Jul 2011

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