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RUNX1 gene mutation in primary myelodysplastic syndrome – the mutation can be detected early at diagnosis or acquired during disease progression and is associated with poor outcome

✍ Scribed by Chien-Yuan Chen; Liang-In Lin; Jih-Luh Tang; Bo-Sheng Ko; Woei Tsay; Wen-Chien Chou; Ming Yao; Shang-Ju Wu; Mei-Hsuan Tseng; Hwei-Fang Tien


Book ID
108675434
Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
306 KB
Volume
139
Category
Article
ISSN
0007-1048

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