Exome sequencing identifies putative drivers of progression of transient myeloproliferative disorder to AMKL in infants with Down syndrome

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Serval ID
serval:BIB_3903B652C0FB
Type
Article: article from journal or magazin.
Collection
Publications
Institution
UNIL/CHUV
Title
Exome sequencing identifies putative drivers of progression of transient myeloproliferative disorder to AMKL in infants with Down syndrome
Journal
Blood
Author(s)
Nikolaev S. I., Santoni F., Vannier A., Falconnet E., Giarin E., Basso G., Hoischen A., Veltman J. A., Groet J., Nizetic D., Antonarakis S. E.
ISSN
1528-0020 (Electronic)
ISSN-L
0006-4971
Publication state
Published
Issued date
2013
Volume
122
Number
4
Pages
554-61
Language
english
Keywords
Cell Transformation, Neoplastic/*genetics, Disease Progression, Down Syndrome/complications/*genetics, Exome/genetics, Genetic Predisposition to Disease/genetics, Genome-Wide Association Study, Genomic Instability/genetics, High-Throughput Nucleotide Sequencing/methods, Humans, Infant, Infant, Newborn, Leukemia, Megakaryoblastic, Acute/complications/*genetics/pathology, Microarray Analysis, Myeloproliferative Disorders/complications/*genetics/pathology, Polymorphism, Single Nucleotide, Transcriptome
OAI-PMH
oai:serval.unil.ch:BIB_3903B652C0FB
DOI
10.1182/blood-2013-03-491936
Pubmed
23733339
Create date
20/05/2019 13:40
Last modification date
14/12/2019 7:26
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