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

Genetic counseling for hereditary cancer syndromes: a 5-year experience from a single center in Bulgaria

保加利亚一家中心五年来的遗传性癌症综合征遗传咨询经验

Hachmeriyan, Mari; Levkova, Mariya; Yahya, Dinnar; Stoyanova, Milena; Dimitrova, Eleonora

Diagnostic Yield of Next-Generation Sequencing for Rare Pediatric Genetic Disorders: A Single-Center Experience

下一代测序技术在罕见儿科遗传疾病诊断中的应用:单中心经验

Stoyanova, Milena; Yahya, Dinnar; Hachmeriyan, Mari; Levkova, Mariya

Clinical Utility of Multiplex Ligation-Dependent Probe Amplification in the Genetic Assessment of Patients with Myelodysplastic Syndrome

多重连接依赖性探针扩增技术在骨髓增生异常综合征患者基因检测中的临床应用

Valeva, Radostina; Levkova, Maria; Yahya, Dinnar; Hachmeriyan, Mari; Micheva, Ilina

Genomic Evaluation of AML-Main Techniques and Novel Approaches

急性髓系白血病基因组评估——主要技术和新方法

Yahya, Dinnar; Stoyanova, Milena; Hachmeriyan, Mari; Levkova, Mariya

Ethical and Psychosocial Issues Associated with Genetic Testing for Hereditary Tumor Predisposition Syndromes

与遗传性肿瘤易感综合征基因检测相关的伦理和社会心理问题

Hachmeriyan, Mari; Levkova, Mariya; Yahya, Dinnar; Stoyanova, Milena; Dimitrova, Eleonora

Multifaceted Primary Ciliary Dyskinesia-A Case Report

多因素原发性纤毛运动障碍——病例报告

Yahya, Dinnar; Benkova-Petrova, Miroslava; Petrov, Aleksandar; Hachmeriyan, Mari

Advances in Chiral Pincer Complexes: Insights and Applications in Catalytic Asymmetric Reactions

手性钳形配合物的研究进展:在催化不对称反应中的见解和应用

Musa, Sanaa; Peretz, Yuval; Dinnar, Gil

NIPT Integration as a Patient-Paid Prenatal Screening Option-Observations and Challenges from a Bulgarian Genetic Counseling Center

NIPT作为患者自费产前筛查方案的整合——来自保加利亚遗传咨询中心的观察与挑战

Yahya, Dinnar; Hachmeriyan, Mari; Stoyanova, Milena; Levkova, Mariya

Myocardial dissection complicating left sinus of Valsalva aneurysm in silent takayasu arteritis

无症状性大动脉炎并发左瓦氏窦动脉瘤合并心肌夹层

Astuti, Astri; Kartamihardja, Achmad Hafiedz Azis; Ilhamy, Muhammad Adniel; Fahlavi, Muhammad Dinnar; Kusumawardhani, Nuraini Yasmin; Hasan, Melawati; Hamijoyo, Laniyati