sgugenetics / -Neurofibromatosis Type 1-
The NF1 gene in tumor syndromes and melanoma | Laboratory Investigation
NF1 Gene Therapy Initiative: Request for Applications | Children's Tumor Foundation
Mutational spectrum of NF1 gene in 24 unrelated Egyptian families with neurofibromatosis type 1 - Abdel‐Aziz - 2021 - Molecular Genetics & Genomic Medicine - Wiley Online Library
IJMS | Free Full-Text | Current Understanding of Neurofibromatosis Type 1, 2, and Schwannomatosis
What is NF - Neurofibromatosis Network
Neurofibromatose type 1 (NF1) – Encore
XL TP53/NF1 - Deletion Probe | MetaSystems Probes
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
Cancers | Free Full-Text | Risk of Optic Pathway Glioma in Neurofibromatosis Type 1: No Evidence of Genotype–Phenotype Correlations in a Large Independent Cohort
Distribution of the identified mutations in the NF1 gene. a Sche- matic... | Download Scientific Diagram
IJMS | Free Full-Text | Current Understanding of Neurofibromatosis Type 1, 2, and Schwannomatosis
Neurofibromatosis Type-1 (NF1) – Decode Genomics
Reprogramming Captures the Genetic and Tumorigenic Properties of Neurofibromatosis Type 1 Plexiform Neurofibromas - ScienceDirect
Neurofibromatosis - Symptoms and causes - Mayo Clinic
Two novel mutations of <i>NF1</i> gene identified in Chinese patients with severe neurofibromatosis type 1 - Indian Journal of Dermatology, Venereology and Leprology
NF1 microdeletions and mutations gene location chromosome 17q11.2
Neurofibromin Is an Estrogen Receptor-α Transcriptional Co-repressor in Breast Cancer - ScienceDirect
Genetics of neurofibromatosis type 1 (NF1)
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PDF] , Monika Gos NeurofibromiN iN Neurofibromatosis type 1 – mutations in NF 1 geNe as a cause of disease * | Semantic Scholar
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
Classification of NF1 microdeletions and its importance for establishing genotype/phenotype correlations in patients with NF1 microdeletions | SpringerLink
Genes | Free Full-Text | Genotype-Phenotype Correlations in Neurofibromatosis Type 1: Identification of Novel and Recurrent NF1 Gene Variants and Correlations with Neurocognitive Phenotype
126 novel mutations in Italian patients with neurofibromatosis type 1 - Bianchessi - 2015 - Molecular Genetics & Genomic Medicine - Wiley Online Library
