SNP array analysis of leukemic relapse samples after allogeneic hematopoietic stem cell transplantation with a sibling donor identifies meiotic recombination spots and reveals possible correlation with the breakpoints of acquired genetic aberrations.

Kajsa Paulsson; David Lindgren; Bertil Johansson

doi:10.1038/leu.2011.79

SNP array analysis of leukemic relapse samples after allogeneic hematopoietic stem cell transplantation with a sibling donor identifies meiotic recombination spots and reveals possible correlation with the breakpoints of acquired genetic aberrations.

Kajsa Paulsson, David Lindgren, Bertil Johansson

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	1358-1361
Journal	Leukemia
Volume	25
DOIs	https://doi.org/10.1038/leu.2011.79
Publication status	Published - 2011

Bibliographical note

Department affilation moved from v1000583 (Molecular Tumour Biology) to v1000562 (Department of Translational Medicine) on 2016-01-18 14:41:46.

Subject classification (UKÄ)

Cancer and Oncology

Access to Document

10.1038/leu.2011.79

http://www.ncbi.nlm.nih.gov/pubmed/21494255?dopt=Abstract

Cite this

@article{651ecd322c634db695ebc59000169bda,

title = "SNP array analysis of leukemic relapse samples after allogeneic hematopoietic stem cell transplantation with a sibling donor identifies meiotic recombination spots and reveals possible correlation with the breakpoints of acquired genetic aberrations.",

author = "Kajsa Paulsson and David Lindgren and Bertil Johansson",

note = "Department affilation moved from v1000583 (Molecular Tumour Biology) to v1000562 (Department of Translational Medicine) on 2016-01-18 14:41:46.",

year = "2011",

doi = "10.1038/leu.2011.79",

language = "English",

volume = "25",

pages = "1358--1361",

journal = "Leukemia",

issn = "1476-5551",

publisher = "Nature Publishing Group",

}

SNP array analysis of leukemic relapse samples after allogeneic hematopoietic stem cell transplantation with a sibling donor identifies meiotic recombination spots and reveals possible correlation with the breakpoints of acquired genetic aberrations. / Paulsson, Kajsa ; Lindgren, David ; Johansson, Bertil.

In: Leukemia, Vol. 25, 2011, p. 1358-1361.

Research output: Contribution to journal › Article › peer-review

TY - JOUR

T1 - SNP array analysis of leukemic relapse samples after allogeneic hematopoietic stem cell transplantation with a sibling donor identifies meiotic recombination spots and reveals possible correlation with the breakpoints of acquired genetic aberrations.

AU - Paulsson, Kajsa

AU - Lindgren, David

AU - Johansson, Bertil

N1 - Department affilation moved from v1000583 (Molecular Tumour Biology) to v1000562 (Department of Translational Medicine) on 2016-01-18 14:41:46.

PY - 2011

Y1 - 2011

U2 - 10.1038/leu.2011.79

DO - 10.1038/leu.2011.79

M3 - Article

C2 - 21494255

VL - 25

SP - 1358

EP - 1361

JO - Leukemia

JF - Leukemia

SN - 1476-5551

ER -