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Open access

Review article

First published 2023

Advances in the Treatment of Rare Epidermal Growth Factor Receptor Mutations in Advanced Nonsmall-Cell Lung Cancer

Limeng Yu, Ruilin Wang, Yuhua Zhao [...]

Technology in Cancer Research & Treatment

Open access

Research article

First published 2024

Analysis of outcomes in resected early-stage NSCLC with rare targetable driver mutations

Nadia Ghazali, Jamie Feng, Katrina Hueniken [...]

Therapeutic Advances in Medical Oncology

Open access

Case report

First published 2025

A rare epidermal growth factor receptor T790M/cis-C797S/L718Q compound mutation in a lung adenocarcinoma patient who did not derive any benefit from combination therapy with afatinib and bevacizumab

Xiaopeng Meng, Jingyi Liu, Xiaohui Wu [...]

Sage Open Medical Case Reports

Retricted access

Research article

First published 1998-1

An Efficient Protocol for Rare Mutation Genotyping in a Large Population

Helmut Zarbl, Corinne Aragaki, Lue Ping Zhao

Genetic Testing and Molecular Biomarkers

Open access

Case report

First published 2023

A Rare Case of Cerebrotendinous Xanthomatosis Associated With a Mutation on COG8 Gene

Hamed Ghoshouni, Roham Sarmadian, Rana Irilouzadian [...]

Journal of Investigative Medicine High Impact Case Reports

Retricted access

Research article

First published 2010-06

Mutation Analysis of the HBB Gene in Selected Bangladeshi β-Thalassemic Individuals: Presence of Rare Mutations

Mustak Ibn Ayub, Mahdi Muhammad Moosa, Golam Sarwardi [...]

Genetic Testing and Molecular Biomarkers

Retricted access

Research article

First published 2010-02

Rare Mutations in the PIK3CA Gene Contribute to Aggressive Endometrial Cancer

Darina Konstantinova, Radka Kaneva, Roumen Dimitrov [...]

DNA and Cell Biology

Open access

Case report

First published 2023

The broad spectrum of tyrosine kinase inhibitors. Treatment of a rare EGFR R776H mutation with Osimertinib: Case report

Joyce Cui, Sana Tabbara, Juskaran Chadha

Sage Open Medical Case Reports

Retricted access

Case report

First published 2025-3

A Rare Case of an Infant With TFE3 Mutation Presenting With Direct Hyperbilirubinemia and Hepatomegaly

Qiong Zhang, Aaron Axelbaum, Katryn Furuya [...]

Pediatric and Developmental Pathology

Retricted access

Research article

First published 2008-09

Assessment of Carriers' Frequency of a Novel MRE11 Mutation Responsible for the Rare Ataxia Telangiectasia-Like Disorder

Ghazi Alsbeih, Khaled Al-Hadyan, Najla Al-Harbi

Genetic Testing and Molecular Biomarkers

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