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

Somatic STAT5b gain-of-function mutations in early onset nonclonal eosinophilia, urticaria, dermatitis, and diarrhea

体细胞STAT5b功能获得性突变与早发性非克隆性嗜酸性粒细胞增多症、荨麻疹、皮炎和腹泻有关

Ma, Chi A; Xi, Liqiang; Cauff, Brian; DeZure, Adam; Freeman, Alexandra F; Hambleton, Sophie; Kleiner, Gary; Leahy, T Ronan; O'Sullivan, Maureen; Makiya, Michelle; O'Regan, Grainne; Pittaluga, Stefania; Niemela, Julie; Stoddard, Jennifer; Rosenzweig, Sergio D; Raffeld, Mark; Klion, Amy D; Milner, Joshua D

Germline SAMD9 mutation in siblings with monosomy 7 and myelodysplastic syndrome

患有 7 号单体和骨髓增生异常综合征的兄弟姐妹中出现种系 SAMD9 突变

J R Schwartz, S Wang, J Ma, T Lamprecht, M Walsh, G Song, S C Raimondi, G Wu, M F Walsh, R B McGee, C Kesserwan, K E Nichols, B E Cauff, R C Ribeiro, M Wlodarski, J M Klco

Transient parvovirus-associated hypoplasia of multiple peripheral blood cell lines in children with chronic hemolytic anemia

慢性溶血性贫血患儿中多种外周血细胞系的短暂性细小病毒相关性发育不良

Cauff, Brian E; Quinn, Charles T