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

Identification of a Novel Homozygous Mutation in PRDM12 Gene in a Patient with Hereditary Sensory and Autonomic Neuropathy Type VIII

在一名患有遗传性感觉和自主神经病 VIII 型的患者中鉴定出 PRDM12 基因的新型纯合突变

Ebrahimi, Amir Hossein; Bolhassani, Manzar; Zarei, Mohammad Reza; Heidari, Matin; ArdeshirDavani, Amin; Mehrtash, Amir Hosein; Shiri, Zahra; Heidari, Masoud; Soleyman-Nejad, Morteza; Taskhiri, Mohammad Hossein; Norouzbeigi, Arefeh; Heidari, Mansour

Prevalence of Chromosomal Abnormalities in Iranian Patients with Infertility

伊朗不孕症患者染色体异常的患病率

Abbaspour, Saima; Isazadeh, Alireza; Heidari, Matin; Heidari, Masoud; Hajazimian, Saba; Soleyman-Nejad, Morteza; Taskhiri, Mohammad Hossein; Bolhassani, Manzar; Ebrahimi, Amir Hossein; Keshavarz, Parvaneh; Shiri, Zahra; Heidari, Mansour

Identification of Two Novel Mutations in PKHD1 Gene from Two Families with Polycystic Kidney Disease by Whole Exome Sequencing

通过全外显子组测序在两个多囊肾病家族中鉴定出PKHD1基因的两个新突变

Heidari, Masoud; Gharshasbi, Hamid; Isazadeh, Alireza; Soleyman-Nejad, Morteza; Taskhiri, Mohammad Hossein; Shapouri, Javad; Bolhassani, Manzar; Sadighi, Nahid; Heidari, Mansour

Association of a novel homozygous mutation in the HMGCS2 gene with an HMGCSD in an Iranian patient

伊朗一名患者中发现HMGCS2基因的新型纯合突变与HMGCSD相关

Heidari, Masoud; Soleyman-Nejad, Morteza; Isazadeh, Alireza; Shapouri, Javad; Taskhiri, Mohammad Hossein; Ahangari, Roghayyeh; Mohamadi, Ali Reza; Ebrahimi, Masoumeh; Karimi, Hadi; Bolhassani, Manzar; Karimi, Zahra; Heidari, Mansour

Identification of Two Novel Mutations in the ATM Gene from Patients with Ataxia-Telangiectasia by Whole Exome Sequencing

通过全外显子组测序鉴定出共济失调毛细血管扩张症患者ATM基因中的两个新突变

Heidari, Masoud; Soleyman-Nejad, Morteza; Taskhiri, Mohammad H; Shahpouri, Javad; Isazadeh, Alireza; Ahangari, Roghayyeh; Mohamadi, Ali R; Ebrahimi, Masoumeh; Karimi, Hadi; Bolhassani, Manzar; Karimi, Zahra; Heidari, Mansour