A molecular analysis of individuals with neurofibromatosis type 1 (NF1) and optic pathway gliomas (OPGs), and an assessment of genotype-phenotype correlations
Author:
Publisher
BMJ
Subject
Genetics (clinical),Genetics
Cited by 82 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Expanding the phenotype of neurofibromatosis type 1 microdeletion syndrome;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2024-07-18
2. An Overview of Optic Pathway Glioma With Neurofibromatosis Type 1: Pathogenesis, Risk Factors, and Therapeutic Strategies;Investigative Ophthalmology & Visual Science;2024-06-05
3. Clinical signs and genetic evaluation of patients with neurofibromatosis type 1 with and without optic pathway gliomas in a center in Turkey;Child's Nervous System;2023-07-04
4. Neurofibromatosis Type 1-Associated Optic Pathway Gliomas: Current Challenges and Future Prospects;Cancer Management and Research;2023-07
5. New insights into the molecular basis of spinal neurofibromatosis type 1;European Journal of Human Genetics;2023-05-22
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