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

A novel variant of ATRX gene is potentially associated with alpha-thalassemia X-linked intellectual disability syndrome: Case report and literature review

ATRX基因的一种新型变异可能与α-地中海贫血X连锁智力障碍综合征相关:病例报告及文献综述

Sarah, Berrada; Amal, Tazzite; Bouchaib, Gazzaz; Hind, Dehbi

A novel SCN8A variant of unknown significance in pediatric epilepsy: a case report

一种与儿童癫痫相关的、意义不明的新型SCN8A变异:病例报告

Bouzroud, Wafaa; Tazzite, Amal; Boussakri, Ikhlass; Gazzaz, Bouchaïb; Dehbi, Hind

R306X Mutation in the MECP2 Gene Causes an Atypical Rett Syndrome in a Moroccan Patient: A Case Report

MECP2基因R306X突变导致摩洛哥患者出现非典型雷特综合征:病例报告

Bouzroud, Wafaa; Tazzite, Amal; Berrada, Sarah; Gazzaz, Bouchaïb; Dehbi, Hind

Next-generation sequencing of BRCA1 and BRCA2 genes in Moroccan prostate cancer patients with positive family history

具有阳性家族史的摩洛哥前列腺癌患者的 BRCA1 和 BRCA2 基因的下一代测序

Fatiha Salmi, Fatima Maachi, Amal Tazzite, Rachid Aboutaib, Jamal Fekkak, Houssine Azeddoug, Hassan Jouhadi

Clinical and pathological features of BRCA1/2 tumors in a sample of high-risk Moroccan breast cancer patients

摩洛哥高危乳腺癌患者样本中BRCA1/2肿瘤的临床和病理特征

Jouhadi, Hassan; Tazzite, Amal; Azeddoug, Houssine; Naim, Asmâa; Nadifi, Sellama; Benider, Abdellatif

Association between ABCB1 C3435T polymorphism and breast cancer risk: a Moroccan case-control study and meta-analysis

ABCB1 C3435T 多态性与乳腺癌风险的关联:一项摩洛哥病例对照研究和荟萃分析

Tazzite, Amal; Kassogue, Yaya; Diakité, Bréhima; Jouhadi, Hassan; Dehbi, Hind; Benider, Abdellatif; Nadifi, Sellama

The CHEK2 1100delC allelic variant is not present in familial and sporadic breast cancer cases from Moroccan population

在摩洛哥人群的家族性和散发性乳腺癌病例中,均未发现 CHEK2 1100delC 等位基因变异。

Marouf, Chaymaa; Hajji, Omar; Diakité, Brehima; Tazzite, Amal; Jouhadi, Hassan; Benider, Abdellatif; Nadifi, Sellama

Methylenetetrahydrofolate reductase C677T polymorphism and breast cancer risk in Moroccan women

亚甲基四氢叶酸还原酶C677T多态性与摩洛哥女性乳腺癌风险

Diakite, B; Tazzite, A; Hamzi, K; Jouhadi, H; Nadifi, S