日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Excess congenital non-synonymous variation in leukemia-associated genes in MLL- infant leukemia: a Children's Oncology Group report

MLL 基因突变导致婴儿白血病中白血病相关基因先天性非同义变异过多:儿童肿瘤协作组报告

Valentine, M C; Linabery, A M; Chasnoff, S; Hughes, A E O; Mallaney, C; Sanchez, N; Giacalone, J; Heerema, N A; Hilden, J M; Spector, L G; Ross, J A; Druley, T E

Genetic variation in MKL2 and decreased downstream PCTAIRE1 expression in extreme, fatal primary human microcephaly.

MKL2 基因变异和下游 PCTAIRE1 表达降低是导致极端致命性原发性人类小头畸形的原因

Ramos E I, Bien-Willner G A, Li J, Hughes A E O, Giacalone J, Chasnoff S, Kulkarni S, Parmacek M, Cole F S, Druley T E