Identification of a common microdeletion cluster in 7q21.3 subband among patients with myeloid leukemia and myelodysplastic syndrome

Author:

Asou Hiroya,Matsui Hirotaka,Ozaki Yuko,Nagamachi Akiko,Nakamura Megumi,Aki Daisuke,Inaba Toshiya

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference18 articles.

1. Refractory anemia, granulocytic hyperplasia of bone marrow, and a missing chromosome in marrow cells. A new clinical syndrome?;Freireich;Clin. Res.,1964

2. Pathology and Genetics of Tumours of Haematopoietic and Lymphoid Tissues;Jaffe,2001

3. Molecular characterization of a myelodysplasia-associated chromosome 7 inversion;Todd;Br. J. Haematol.,2001

4. Single nucleotide polymorphism array analysis of cancer;Dutt;Curr. Opin. Oncol.,2007

5. DNA copy-number analysis of the 22q11 deletion-syndrome region using array-CGH with genomic and PCR-based targets;Mantripragada;Int. J. Mol. Med.,2004

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