Results 171 to 180 of about 30,324 (227)

Identification of cryptic breakpoints through single-tube long fragment read whole genome sequencing based on preimplantation genetic testing. [PDF]

open access: yesNPJ Genom Med
Jiang L   +12 more
europepmc   +1 more source

A Case of Intracranial Mesenchymal Tumor, FET::CREB Fusion-positive, Diagnosed by Genomic Profiling with FoundationOne CDx. [PDF]

open access: yesNMC Case Rep J
Sono K   +7 more
europepmc   +1 more source

Utility of Optical Genome Mapping for Accurate Detection and Fine-Mapping of Structural Variants in Elusive Rare Diseases. [PDF]

open access: yesInt J Mol Sci
Orellana C   +10 more
europepmc   +1 more source

Polymorphisms in the MLL breakpoint cluster region (BCR)

Human Genetics, 2003
The MLL gene is involved in many chromosomal translocations leading to both acute myeloid and lymphoid leukemia. Some patients treated for primary malignancies with chemotherapeutic agents that inhibit DNA topoisomerase II (topo II) develop treatment-related leukemia (t-AML) caused by MLL gene rearrangement.
Richard A. Larson   +16 more
openaire   +3 more sources

The genomic breakpoint in a patient with Philadelphia-positive acute leukemia is 5′ of the breakpoint cluster region

Cancer Genetics and Cytogenetics, 1988
We report a case of acute leukemia in which studies at presentation showed both myeloid and lymphoid cell surface markers. At relapse membrane markers studies were consistent with a leukemia of B-lymphoid lineage. However, immunoglobulin (Ig) and T cell receptor (TCR) beta chain genes were both found in a rearranged configuration.
Lucio Luzzatto   +9 more
openaire   +3 more sources

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