Distribution of the identified mutations in the NF1 gene. a Sche- matic... | Download Scientific Diagram
Neurofibromatosis Type-1 (NF1) – Decode Genomics
Neurofibromatosis - Symptoms and causes - Mayo Clinic
What is NF - Neurofibromatosis Network
Genetic diagnosis of neurofibromatosis type 1: targeted next- generation sequencing with Multiple Ligation-Dependent Probe Amplification analysis | Journal of Biomedical Science | Full Text
Distribution of NF1 gene mutations in neurofibromatosis type 1... | Download Scientific Diagram
Identification and characterization of NF1 and non-NF1 congenital pseudarthrosis of the tibia based on germline NF1 variants: genetic and clinical analysis of 75 patients | Orphanet Journal of Rare Diseases | Full Text
AstraZeneca on Twitter: "Neurofibromatosis type 1 (NF1) is often inherited from a parent. However, 30-50% of new cases are caused by a spontaneous mutation of the #NF1 gene. https://t.co/8I0QiKYNTt" / Twitter
NF1 Tumor Suppressor Gene Function: Cell
Frontiers | Molecular Diagnosis of Neurofibromatosis by Multigene Panel Testing
IJMS | Free Full-Text | Current Understanding of Neurofibromatosis Type 1, 2, and Schwannomatosis
Genetics of neurofibromatosis type 1 (NF1)
NF1 Associated with More Cancer Types Than Previously Known - NCI
NF1 GENE DELETION
Two novel mutations of <i>NF1</i> gene identified in Chinese patients with severe neurofibromatosis type 1 - Indian Journal of Dermatology, Venereology and Leprology
Neurofibromatosis type 1 associated low grade gliomas: A comparison with sporadic low grade gliomas - ScienceDirect
Neurofibromatosis Genetic Testing
126 novel mutations in Italian patients with neurofibromatosis type 1 - Bianchessi - 2015 - Molecular Genetics & Genomic Medicine - Wiley Online Library
GIST with a NF1 mutation | GIST Support International
Independent NF1 mutations underlie café-au-lait macule development in a woman with segmental NF1 | Neurology Genetics
NF1 Gene - GeneCards | NF1 Protein | NF1 Antibody
Neurofibromatosis Type 1 Due to Germ-Line Mosaicism in a Clinically Normal Father | NEJM
Classification of NF1 microdeletions and its importance for establishing genotype/phenotype correlations in patients with NF1 microdeletions | SpringerLink
Mutational spectrum of NF1 gene in 24 unrelated Egyptian families with neurofibromatosis type 1 - Abdel‐Aziz - 2021 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Growth Regulation in the Nervous System | Gutmann Research Laboratory | Washington University in St. Louis
Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation | Genetics in Medicine
Cancers | Free Full-Text | Risk of Optic Pathway Glioma in Neurofibromatosis Type 1: No Evidence of Genotype–Phenotype Correlations in a Large Independent Cohort
John Libbey Eurotext - European Journal of Dermatology - Neurofibromatosis type 1 and X-linked ichthyosis in a patient with a novel frameshift mutation in the NF1 gene
