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Submicroscopic deletion of FGFR1 gene is recurrently detected in myeloid and lymphoid neoplasms associated with ZMYM2-FGFR1 rearrangements: a case study

Authors
 Yang J.J.  ;  Park T.S.  ;  Choi J.R.  ;  Park S.-J.  ;  Cho S.Y.  ;  Jun K.R.  ;  Kim H.R.  ;  Lee J.N.  ;  Oh S.H.  ;  Lee S.  ;  Kim B.  ;  Marschalek R.  ;  Meyer C. 
Citation
 ACTA HAEMATOLOGICA, Vol.127(2) : 119-123, 2012 
Journal Title
ACTA HAEMATOLOGICA
ISSN
 0001-5792 
Issue Date
2012
MeSH
Base Sequence ; Chromosome Deletion ; Chromosomes, Human, Pair 8/genetics ; DNA-Binding Proteins/genetics* ; Fatal Outcome ; Gene Deletion* ; Gene Rearrangement* ; Humans ; Male ; Middle Aged ; Molecular Sequence Data ; Myeloproliferative Disorders/genetics* ; Receptor, Fibroblast Growth Factor, Type 1/genetics* ; Transcription Factors/genetics*
Keywords
Base Sequence ; Chromosome Deletion ; Chromosomes, Human, Pair 8/genetics ; DNA-Binding Proteins/genetics* ; Fatal Outcome ; Gene Deletion* ; Gene Rearrangement* ; Humans ; Male ; Middle Aged ; Molecular Sequence Data ; Myeloproliferative Disorders/genetics* ; Receptor, Fibroblast Growth Factor, Type 1/genetics* ; Transcription Factors/genetics*
Full Text
http://www.karger.com/Article/Abstract/334707
DOI
22236811
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Laboratory Medicine (진단검사의학교실) > 1. Journal Papers
Yonsei Authors
Park, Seo Jin(박서진)
Choi, Jong Rak(최종락) ORCID logo https://orcid.org/0000-0002-0608-2989
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/89362
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