A case with a cytogenetically cryptic variant of the inv(16)(p13q22)/t(16;16)(p13;q22)

Cancer Genet. 2014 May;207(5):231-2. doi: 10.1016/j.cancergen.2014.04.009. Epub 2014 May 4.

Authors

Florence Van Obbergh¹, Lucienne Michaux¹, Johan Maertens², Hélène Schoemans², Peter Vandenberghe³

Affiliations

¹ Center for Human Genetics, University Hospital Leuven and KU Leuven, Leuven, Belgium.
² Department of Hematology, University Hospital Leuven and KU Leuven, Leuven, Belgium.
³ Center for Human Genetics and Department of Hematology, University Hospital Leuven and KU Leuven, Leuven, Belgium. Electronic address: [email protected].

PMID: 24972931
DOI: 10.1016/j.cancergen.2014.04.009

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Chromosome Inversion / genetics*
Chromosomes, Human, Pair 16 / genetics*
Core Binding Factor beta Subunit / genetics*
Female
Humans
Leukemia, Myeloid, Acute / genetics*
Middle Aged
Mutagenesis, Insertional
Myosin Heavy Chains / genetics*

Substances

CBFB protein, human
Core Binding Factor beta Subunit
MYH11 protein, human
Myosin Heavy Chains