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

Whole Exome Sequencing in Patients With Developmental Delay/Intellectual Disability (DD/ID), Epilepsy and the First Turkish Patient Diagnosed With BCL11A-Related Intellectual Disability

对发育迟缓/智力障碍(DD/ID)、癫痫患者以及首例被诊断为BCL11A相关智力障碍的土耳其患者进行全外显子组测序

Akkus, Nejmiye; Canbal, Abdullah; Guneysu, Seda; Gokce, Erkan; Duzgun, Pakize; Barıs, İbrahim

Unveiling the role of miRNA in laryngeal squamous cell carcinoma progression: a retrospective study

揭示miRNA在喉鳞状细胞癌进展中的作用:一项回顾性研究

Akkuş, Nejmiye; Kaya Çelik, Elif; Ozdemir, Suleyman; Sapmaz, Emrah

First Clinical Report of Two RAB3GAP1 Pathogenic Variant in Warburg Micro Syndrome

瓦尔堡微综合征中两种 RAB3GAP1 致病变异的首例临床报告

Akkuş, Nejmiye; Duman, Tuğba Akın

Germline landscape of BRCAs by 7-site collaborations as a BRCA consortium in Turkey

土耳其 BRCA 联盟通过 7 个研究中心合作开展的 BRCA 基因系图谱研究

Bisgin, Atil; Sag, Sebnem Ozemri; Dogan, Muhammet E; Yildirim, Mahmut S; Gumus, Aydeniz Aydin; Akkus, Nejmiye; Balasar, Ozgur; Durmaz, Ceren D; Eroz, Recep; Altiner, Sule; Alemdar, Adem; Aliyeva, Lamia; Boga, Ibrahim; Cam, Fethi S; Dogan, Berkcan; Esbah, Onur; Hanta, Abdullah; Mujde, Cem; Ornek, Cemre; Ozer, Sinem; Rencuzogullari, Cagla; Sonmezler, Ozge; Bozdogan, Sevcan Tug; Dundar, Munis; Temel, Sehime G

Smith-Magenis Syndrome: Clues in the Clinic

史密斯-马吉尼斯综合征:临床线索

Akkus, Nejmiye; Kilic, Betul; Cubuk, Pelin Ozyavuz

Recombinant chromosome with partial 14 q trisomy due to maternal pericentric inversion

由于母源性臂间倒位导致的重组染色体,具有部分14q三体性

Kurtulgan, Hande Küçük; Özer, Leyla; Yıldırım, Malik Ejder; Ünsal, Evrim; Aktuna, Süleyman; Baltacı, Volkan; Akkuş, Nejmiye; Sezgin, İlhan