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

RAD51C mutation screening in high-risk patients from Serbian hereditary breast/ovarian cancer families

对塞尔维亚遗传性乳腺癌/卵巢癌家族的高危患者进行RAD51C基因突变筛查

Krivokuca, Ana; Yanowski, Kira; Rakobradovic, Jelena; Benitez, Javier; Brankovic-Magic, Mirjana

Combined NGS approaches identify mutations in the intraflagellar transport gene IFT140 in skeletal ciliopathies with early progressive kidney Disease

结合NGS技术可识别骨骼纤毛病伴早期进行性肾病中鞭毛内转运基因IFT140的突变

Schmidts, Miriam; Frank, Valeska; Eisenberger, Tobias; Al Turki, Saeed; Bizet, Albane A; Antony, Dinu; Rix, Suzanne; Decker, Christian; Bachmann, Nadine; Bald, Martin; Vinke, Tobias; Toenshoff, Burkhard; Di Donato, Natalia; Neuhann, Theresa; Hartley, Jane L; Maher, Eamonn R; Bogdanović, Radovan; Peco-Antić, Amira; Mache, Christoph; Hurles, Matthew E; Joksić, Ivana; Guć-Šćekić, Marija; Dobricic, Jelena; Brankovic-Magic, Mirjana; Bolz, Hanno J; Pazour, Gregory J; Beales, Philip L; Scambler, Peter J; Saunier, Sophie; Mitchison, Hannah M; Bergmann, Carsten

Screening of the DNA mismatch repair genes MLH1, MSH2 and MSH6 in a Greek cohort of Lynch syndrome suspected families

在希腊林奇综合征疑似家系中筛查 DNA 错配修复基因 MLH1、MSH2 和 MSH6

Georgia Thodi, Florentia Fostira, Raphael Sandaltzopoulos, George Nasioulas, Anastasios Grivas, Ioannis Boukovinas, Maria Mylonaki, Christos Panopoulos, Mirjana Brankovic Magic, George Fountzilas, Drakoulis Yannoukakos

BRCA Testing in Serbia and Montenegro

塞尔维亚和黑山的 BRCA 基因检测

Brankovic-Magic, Mirjana