Identification and characterization of sporadic and inherited mutations in exon 31 of the neurofibromatosis (NF1) gene
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00222716.pdf
Cited by 25 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. Clinical and molecular characteristics of thirty NF1 variants in Chinese patients with neurofibromatosis type 1;Molecular Biology Reports;2019-06-14
2. Characterization of early communicative behavior in mouse models of neurofibromatosis type 1;Autism Research;2017-08-26
3. Neurofibromatosis-Noonan Syndrome: A Possible Paradigm of the Combination of Genetic and Epigenetic Factors;Advances in Experimental Medicine and Biology;2017
4. Neurofibromin and NF1 Gene Analysis in Composite Pheochromocytoma and Tumors Associated with von Recklinghausen’s Disease;Modern Pathology;2002-03
5. Allele-Specific Non-CpG Methylation of the Nf1 Gene during Early Mouse Development;Developmental Biology;2001-12
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