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

Oculocutaneous albinism in a patient with an OCA2 variant: molecular and clinical insights

OCA2变异患者的眼皮肤白化病:分子和临床见解

Neissi, Mostafa; Al-Mozani, Sahar Kareem; Al-Zaalan, Ayoob Radhi; Sanavi Shiri, Samaneh; Sheikh-Hosseini, Motahareh; Al-Badran, Adnan Issa; Nekouei, Elaheh

Identification and characterization of NMNAT1 gene mutations in an Iranian patient with Leber congenital amaurosis 9

对一名患有 Leber 先天性黑蒙的伊朗患者进行 NMNAT1 基因突变的鉴定和表征 9

Neissi, Mostafa; Sheikh-Hosseini, Motahareh; Mohammadi-Asl, Misagh; Al-Badran, Adnan Issa; Roghani, Mojdeh; Mohammadi-Asl, Javad; Jorfi, Kamele

Y-chromosome variation in Basrah population

巴士拉人群的Y染色体变异

Ohied, Bassim Muften; Al-Badran, Adnan Issa

Screening of LEP gene polymorphisms as a risk factor for obesity and type 2 diabetes in Iraqis

筛查LEP基因多态性作为伊拉克人肥胖和2型糖尿病的风险因素

Almyah, Maysoon Khudheyer; Albadran, Adnan Issa