Neurofibromatosis - Symptoms and causes - Mayo Clinic
Genetics of neurofibromatosis type 1 (NF1)
XL TP53/NF1 - Deletion Probe | MetaSystems Probes
Recurrent mutations in the NF1 gene are common among neurofibromatosis type 1 patients | Journal of Medical Genetics
IJMS | Free Full-Text | Current Understanding of Neurofibromatosis Type 1, 2, and Schwannomatosis
126 novel mutations in Italian patients with neurofibromatosis type 1 - Bianchessi - 2015 - Molecular Genetics & Genomic Medicine - Wiley Online Library
sgugenetics / -Neurofibromatosis Type 1-
Mutational spectrum of NF1 gene in 24 unrelated Egyptian families with neurofibromatosis type 1 - Abdel‐Aziz - 2021 - Molecular Genetics & Genomic Medicine - Wiley Online Library
The NF1 mutation categories and distribution. Notes: (A) Mutation... | Download Scientific Diagram
Independent NF1 mutations underlie café-au-lait macule development in a woman with segmental NF1 | Neurology Genetics
Neurofibromatosis Type-1 (NF1) – Decode Genomics
Neurofibromin Is an Estrogen Receptor-α Transcriptional Co-repressor in Breast Cancer - ScienceDirect
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 (NF1) – Decode Genomics
Frontiers | Impacts of NF1 Gene Mutations and Genetic Modifiers in Neurofibromatosis Type 1
Frontiers | Molecular Diagnosis of Neurofibromatosis by Multigene Panel Testing
Distribution of the identified mutations in the NF1 gene. a Sche- matic... | Download Scientific Diagram
Genetic diagnosis of neurofibromatosis type 1: targeted next- generation sequencing with Multiple Ligation-Dependent Probe Amplification analysis | Journal of Biomedical Science | Full Text
NF1 GENE DELETION
Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation | Genetics in Medicine