Concurrent somatic KRAS mutation and germline 10q22.3-q23.2 deletion in a patient with juvenile myelomonocytic leukemia, developmental delay, and multiple malformations: a case report

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作者
Ruen Yao
Tingting Yu
Yufei Xu
Guoqiang Li
Lei Yin
Yunfang Zhou
Jian Wang
Zhilong Yan
机构
[1] Shanghai Jiao Tong University School of Medicine,Department of Medical Genetics and Molecular Diagnostic Laboratory, Shanghai Children’s Medical Center
[2] Shanghai Jiaotong University School of Medicine,Institute for Pediatric Translational Medicine, Shanghai Children’s Medical Center
[3] Shanghai Jiaotong University School of Medicine,Department of Internal Medicine, Shanghai Children’s Medical Center
[4] Shanghai Jiaotong University School of Medicine,Rare Diseases Outpatient Clinic, Shanghai Children’s Medical Center
[5] Shanghai Jiaotong University School of Medicine,Department of Pediatric Surgery, Shanghai Children’s Medical Center
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KRAS; 10q deletion; Juvenile myelomonocytic leukemia; Developmental delay; Whole-exome sequencing;
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