Submicroscopic Deletion of <i>FGFR1</i> Gene Is Recurrently Detected in Myeloid and Lymphoid Neoplasms Associated with <i>ZMYM2-FGFR1</i> Rearrangements: A Case Study-Reference-Cited by-同舟云学术

Submicroscopic Deletion of FGFR1 Gene Is Recurrently Detected in Myeloid and Lymphoid Neoplasms Associated with ZMYM2-FGFR1 Rearrangements: A Case Study

Published:2012 Issue:2 Volume:127 Page:119-123
ISSN:0001-5792
Container-title:Acta Haematologica
language:en
Short-container-title:Acta Haematol

Author:

Yang John Jeongseok,Park Tae Sung,Choi Jong Rak,Park Seo-Jin,Cho Sun Young,Jun Kyung Ran,Kim Hye Ran,Lee Jeong Nyeo,Oh Seung Hwan,Lee Sanggyu,Kim Bomi,Marschalek Rolf,Meyer Claus

Publisher

S. Karger AG

Subject

Hematology,General Medicine

Reference21 articles.

1. The 8p11 Myeloproliferative Syndrome: A Distinct Clinical Entity Caused by Constitutive Activation of FGFR1

2. 8p11 myeloproliferative syndrome: a review

3. Fibroblast growth factor receptor 1 is fused to FIM in stem-cell myeloproliferative disorder with t(8;13)(p12;q12)

4. Consistent Fusion of ZNF198 to the Fibroblast Growth Factor Receptor-1 in the t(8;13)(p11;q12) Myeloproliferative Syndrome

5. PKC412 inhibits the zinc finger 198-fibroblast growth factor receptor 1 fusion tyrosine kinase and is active in treatment of stem cell myeloproliferative disorder

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2. Identification of genomic aberrations in hemangioblastoma by droplet digital PCR and SNP microarray highlights novel candidate genes and pathways for pathogenesis;BMC Genomics;2016-01-14

3. 8p11 Myeloproliferative Syndrome with t(7;8) Translocation Presenting as Acute Myeloid Leukemia: A Case Report and Literature Review;Acta Haematologica;2016

4. 8p11 Myeloproliferative Syndrome with t(1;8)(q25;p11.2): A Case Report and Review of the Literature;Acta Haematologica;2014-09-16

5. RE: Acute myeloid leukemia associated with FGFR1 abnormalities;International Journal of Hematology;2013-06-07