Cargando…
Evidence-based genomic diagnosis characterized chromosomal and cryptic imbalances in 30 elderly patients with myelodysplastic syndrome and acute myeloid leukemia
BACKGROUND: To evaluate the clinical validity of genome-wide oligonucleotide array comparative genomic hybridization (aCGH) for detecting somatic abnormalities, we have applied this genomic analysis to 30 cases (13 MDS and 17 AML) with clonal chromosomal abnormalities detected in more than 50% of an...
Autores principales: | Bajaj, Renu, Xu, Fang, Xiang, Bixia, Wilcox, Katherine, DiAdamo, Autumn J, Kumar, Rachana, Pietraszkiewicz, Alexandra, Halene, Stephanie, Li, Peining |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3031273/ https://www.ncbi.nlm.nih.gov/pubmed/21251322 http://dx.doi.org/10.1186/1755-8166-4-3 |
Ejemplares similares
-
Jumping Translocations of 1q in Myelodysplastic Syndrome and Acute Myeloid Leukemia: Report of Three Cases and Review of Literature
por: Couture, T., et al.
Publicado: (2018) -
Cytogenomic Characterization of Giant Ring or Rod Marker Chromosome in Four Cases of Well-Differentiated and Dedifferentiated Liposarcoma
por: Chai, Hongyan, et al.
Publicado: (2022) -
Changes in and Efficacies of Indications for Invasive Prenatal Diagnosis of Cytogenomic Abnormalities: 13 Years of Experience in a Single Center
por: Meng, Jinlai, et al.
Publicado: (2015) -
Inverted duplication, triplication and quintuplication through sequential breakage‐fusion‐bridge events induced by a terminal deletion at 5p in a case of spontaneous abortion
por: Chai, Hongyan, et al.
Publicado: (2019) -
Analytical validation and chromosomal distribution of regions of homozygosity by oligonucleotide array comparative genomic hybridization from normal prenatal and postnatal case series
por: Wen, Jiadi, et al.
Publicado: (2019)