Mosaicism in sporadic neurofibromatosis type 1: variations on a theme common to other hereditary cancer syndromes?
Author:
Publisher
BMJ
Subject
Genetics (clinical),Genetics
Cited by 69 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. Childhood-Onset Refractory Hypertension Results from Neurofibromatosis Type 1 Caused by a Splicing <i>NF1</i> Mutation;Kidney and Blood Pressure Research;2023
2. Cancer Causative Mutations Occurring in Early Embryogenesis;Cancer Discovery;2021-12-23
3. Impacts of NF1 Gene Mutations and Genetic Modifiers in Neurofibromatosis Type 1;Frontiers in Neurology;2021-09-08
4. Pheochromocytoma and Paraganglioma;The Hereditary Basis of Childhood Cancer;2021
5. Sporadic and Familial Variants in NF1: An Explanation of the Wide Variability in Neurocognitive Phenotype?;Frontiers in Neurology;2020-05-05
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