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A Novel Variant Rearrangement of the Rare Aberration dic(17;20)(p11.2;q11.2) Characterized by Array-CGH as an Insertion in a Patient with Myelodysplastic Syndrome of Multilineage Dysplasia (MDS-MLD)

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关键词 17p deletion 20q deletion Dic(17 20)Insertion Myelodysplastic syndrome

发布时间 2020-08-12

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Cytogenetic and genome research

2020年160卷1期

22-28页

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Cytogenetic and genome research

2020年160卷1期

22-28页

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A Novel Variant Rearrangement of the Rare Aberration dic(17;20)(p11.2;q11.2) Characterized by Array-CGH as an Insertion in a Patient with Myelodysplastic Syndrome of Multilineage Dysplasia (MDS-MLD)

Cytogenetic and genome research

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A Novel Variant Rearrangement of the Rare Aberration dic(17;20)(p11.2;q11.2) Characterized by Array-CGH as an Insertion in a Patient with Myelodysplastic Syndrome of Multilineage Dysplasia (MDS-MLD)

Cytogenetic and genome research

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Cytogenetic and genome research

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