Rapid next-generation sequencing aids in diagnosis of transient abnormal myelopoiesis in a phenotypically normal newborn-Reference-Cited by-同舟云学术

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

Published:2022-05-06 Issue:9 Volume:6 Page:2893-2896
ISSN:2473-9529
Container-title:Blood Advances
language:en
Short-container-title:

Author:

Aziz-Bose Rahela¹²³^ORCID,Wachter Franziska¹²³,Chiarle Roberto²⁴^ORCID,Lindeman Neal I.²⁵,Kim Annette S.²⁵^ORCID,Degar Barbara A.¹²³,Davies Kimberly¹²³,Pikman Yana¹²³^ORCID

Affiliation:

1. Department of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA;

2. Harvard Medical School, Boston, MA;

3. Division of Hematology/Oncology, Boston Children's Hospital, Boston, MA,

4. Department of Pathology, Boston Children’s Hospital, Boston, MA; and

5. Department of Pathology, Brigham and Women’s Hospital, Boston, MA

Publisher

American Society of Hematology

Subject

Hematology

Link

https://ashpublications.org/bloodadvances/article-pdf/6/9/2893/1895188/advancesadv2021006865.pdf

Reference22 articles.

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2. Acquired mutations in GATA1 in the megakaryoblastic leukemia of Down syndrome;Wechsler;Nat Genet.,2002

3. Frequent mutations in the GATA-1 gene in the transient myeloproliferative disorder of Down syndrome;Xu;Blood.,2003

4. Functional profiling of single CRISPR/Cas9-edited human long-term hematopoietic stem cells;Wagenblast;Nat Commun,2019

5. GATA1-related leukaemias;Shimizu;Nat Rev Cancer.,2008

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