Rapid next-generation sequencing aids in diagnosis of transient abnormal myelopoiesis in a phenotypically normal newborn.

TitleRapid next-generation sequencing aids in diagnosis of transient abnormal myelopoiesis in a phenotypically normal newborn.
Publication TypeJournal Article
Year of Publication2022
AuthorsAziz-Bose R, Wachter F, Chiarle R, Lindeman NI, Kim AS, Degar BA, Davies K, Pikman Y
JournalBlood Adv
Volume6
Issue9
Pagination2893-2896
Date Published2022 May 10
ISSN2473-9537
KeywordsDown Syndrome, High-Throughput Nucleotide Sequencing, Humans, Infant, Newborn, Leukemoid Reaction
DOI10.1182/bloodadvances.2021006865
Alternate JournalBlood Adv
PubMed ID35090166
PubMed Central IDPMC9092404
Grant ListK08 CA222684 / CA / NCI NIH HHS / United States
P50 CA206963 / CA / NCI NIH HHS / United States
T32 CA136432 / CA / NCI NIH HHS / United States
Related Faculty: 
Neal Lindeman, M.D.

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