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

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ID Serval
serval:BIB_3903B652C0FB
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
UNIL/CHUV
Titre
Exome sequencing identifies putative drivers of progression of transient myeloproliferative disorder to AMKL in infants with Down syndrome
Périodique
Blood
Auteur⸱e⸱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
Statut éditorial
Publié
Date de publication
2013
Volume
122
Numéro
4
Pages
554-61
Langue
anglais
Mots-clé
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
Création de la notice
20/05/2019 13:40
Dernière modification de la notice
14/12/2019 7:26
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