Isodicentric (X)(q13): A new characteristic chromosomal anomaly in myeloproliferative syndrome?
Author:
Publisher
Elsevier BV
Subject
Cancer Research,Genetics,Molecular Biology
Reference3 articles.
1. Three patients with structurally abnormal X chromosomes, each with (X)(q13) break points and a history of idiopathic acquired side-roblastic anemia;Dewald;Blood,1981
2. Dysmyelopoietic syndrome: Sequential clinical and cytogenetic studies;Streuli;Blood,1980
3. The chromosomes in human cancer and leukemia;Sandberg,1980
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1. Isochromosome X in Myelodysplastic Syndrome;Acta Haematologica;2015-08-22
2. Loss of ABCB7 gene: pathogenesis of mitochondrial iron accumulation in erythroblasts in refractory anemia with ringed sideroblast with isodicentric (X)(q13);International Journal of Hematology;2011-03
3. The idic(X)(q13) in myeloid malignancies: breakpoint clustering in segmental duplications and association with TET2 mutations;Human Molecular Genetics;2010-01-21
4. Monosomy X as a recurring sole cytogenetic abnormality associated with myelodysplastic diseases;Cancer Genetics and Cytogenetics;1997-02
5. Myelodysplasia Associated with Turner Syndrome;Journal of Pediatric Hematology/Oncology;1996-08
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