Parental origin of monosomic chromosomes in near-haploid acute lymphoblastic leukemia
Blood Cancer J
.
2020 May 5;10(5):51.
doi: 10.1038/s41408-020-0317-2.
Authors
Kristina B Lundin-Ström
1
,
Kristoffer Ström
2
,
Andrea Biloglav
3
,
Gisela Barbany
4
,
Mikael Behrendtz
5
,
Anders Castor
6
,
Linda Olsson-Arvidsson
3
7
,
Bertil Johansson
3
7
Affiliations
1
Division of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden. kristina.lundin_strom@med.lu.se.
2
Lund University Diabetes Centre, Department of Clinical Sciences, Lund University, Malmö, Sweden.
3
Division of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden.
4
Department of Molecular Medicine and Surgery, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden.
5
Department of Pediatrics, Linköping University Hospital, Linköping, Sweden.
6
Department of Pediatrics, Skåne University Hospital, Lund, Sweden.
7
Department of Clinical Genetics and Pathology, Division of Laboratory Medicine, Lund, Sweden.
PMID:
32371983
PMCID:
PMC7200744
DOI:
10.1038/s41408-020-0317-2
No abstract available
Publication types
Letter
MeSH terms
Female
Genomic Imprinting
Haploidy*
Humans
Male
Monosomy*
Pedigree
Precursor Cell Lymphoblastic Leukemia-Lymphoma / genetics*
Grants and funding
PR2018-0004/Barncancerfonden (Swedish Childhood Cancer Foundation)/International
CAN 2017/291/Cancerfonden (Swedish Cancer Society)/International
2016-01084/Vetenskapsrådet (Swedish Research Council)/International