Lv12
90 积分 2022-05-06 加入
A unique presentation of T‐lymphoblastic lymphoma in a pediatric patient with a germline RUNX1 mutation
2小时前
待确认
Bone Marrow Morphology Associated With GermlineRUNX1Mutations in Patients With Familial Platelet Disorder With Associated Myeloid Malignancy
2小时前
已关闭
LIS1-associated classic lissencephaly: A retrospective, multicenter survey of the epileptogenic phenotype and response to antiepileptic drugs
9小时前
已完结
[A new EXT2 mutation in a Chinese family with hereditary multiple exostoses]
1个月前
已完结
ASC1 complex related conditions: Two novel paediatric patients with TRIP4 pathogenic variants and review of literature
1个月前
已完结
A case of rare splice-site Bruton's tyrosine kinase mutation with atypical X-linked agammaglobulinemia
1个月前
已关闭
Mutation spectrum of amyotrophic lateral sclerosis in Central South China
1个月前
已完结
Clinical and genetic spectra of 1550 index patients with hereditary spastic paraplegia
1个月前
已完结
Differences in cancer prevalence among CHEK2 carriers identified via multi-gene panel testing
1个月前
已完结
Prevalence of pathogenic germline cancer risk variants in testicular cancer patients: Identifying high risk groups
1个月前
已完结
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