| Q41677655 | A 90 kb DNA deletion associated with neurofibromatosis type 1. |
| Q33963473 | A chromosome jump crosses a translocation breakpoint in the von Recklinghausen neurofibromatosis region |
| Q48206401 | A small deletion and an adjacent base exchange in a potential stem-loop region of the neurofibromatosis 1 gene |
| Q27000191 | Autophagy in malignant transformation and cancer progression |
| Q24633977 | Characterization of complex chromosomal rearrangements by targeted capture and next-generation sequencing |
| Q30531015 | Chromosome 17p deletions and p53 gene mutations associated with the formation of malignant neurofibrosarcomas in von Recklinghausen neurofibromatosis |
| Q30503427 | Clinical and genetic patterns of neurofibromatosis 1 and 2. |
| Q31138286 | Complete physical map and gene content of the human NF1 tumor suppressor region in human and mouse |
| Q35889608 | Cytologically balanced t(2;20) in a two-generation family with alagille syndrome: cytogenetic and molecular studies. |
| Q44718557 | Differential effects of neurofibromin gene dosage on melanocyte development |
| Q41123138 | Familial neurofibromatosis type 1: clinical experience with DNA testing |
| Q71867165 | Familial reciprocal translocation t(17;19) (q11.2;q13.2) associated with neurofibromatosis type 1, including one patient with non-Hodgkin lymphoma and an additional t(14;20) in B lymphocytes |
| Q33782987 | Genetic and physical map of the von Recklinghausen neurofibromatosis (NF1) region on chromosome 17. |
| Q34652658 | Genetic interactions between neurofibromin and endothelin receptor B in mice |
| Q33534212 | Gliomas |
| Q37064070 | Identification and characterization of the gene for neurofibromatosis type 1 |
| Q40791054 | Identification of candidate genes on chromosome band 20q12 by physical mapping of translocation breakpoints found in myeloid leukemia cell lines |
| Q41236837 | Interphase cytogenetic analysis of solid tumors by non-isotopic DNA in situ hybridization |
| Q33594500 | Large de novo DNA deletion in a patient with sporadic neurofibromatosis 1, mental retardation, and dysmorphism |
| Q31162099 | Long-distance restriction mapping of the proximal long arm of human chromosome 21 with Not I linking clones |
| Q68048424 | Long-range physical mapping of the alpha-amylase-1 (alpha-Amy-1) loci on homoeologous group 6 chromosomes of wheat |
| Q52425277 | Malignant Peripheral Nerve Sheath Tumors. |
| Q37003276 | Molecular Genetics of von Recklinghausen Neurofibromatosis |
| Q37719525 | Molecular and cellular mechanisms of learning disabilities: a focus on NF1. |
| Q41163434 | Molecular and cytogenetic analysis of tumors in von Recklinghausen neurofibromatosis |
| Q41626535 | Molecular aspects of neuro-oncology |
| Q41685840 | Molecular assignment of a translocation breakpoint in acute myeloid leukemia with t(8;21). |
| Q28241993 | Molecular basis of neurofibromatosis type 1 (NF1): mutation analysis and polymorphisms in the NF1 gene |
| Q41131665 | Molecular biology of pediatric gliomas |
| Q41590695 | Molecular characterization of a 17q11.2 translocation in a malignant schwannoma cell line |
| Q40312021 | Molecular characterization of a novel translocation t(5;14)(q21;q32) in a patient with congenital abnormalities |
| Q24518449 | Molecular genetics of neurofibromatosis type 1 (NF1) |
| Q35195336 | Multicolor in situ hybridization and linkage analysis order Charcot-Marie-Tooth type I (CMTIA) gene-region markers |
| Q28217299 | Neurocutaneous disorders |
| Q36941613 | Neurofibromatosis type 1 (NF1) gene: implication in neuroectodermal differentiation and genesis of brain tumors |
| Q28279834 | Neurofibromatosis type 1: piecing the puzzle together |
| Q30449267 | Neurofibromatosis: chronological history and current issues |
| Q77752534 | Parallels between tuberous sclerosis complex and neurofibromatosis 1: common threads in the same tapestry |
| Q36960893 | Pathogenesis of plexiform neurofibroma: tumor-stromal/hematopoietic interactions in tumor progression |
| Q22061729 | Phosphoproteomic Analysis of the Mouse Brain Cytosol Reveals a Predominance of Protein Phosphorylation in Regions of Intrinsic Sequence Disorder |
| Q37610074 | Prenatal diagnosis of the neurofibromatoses. |
| Q36476833 | Progress toward the Isolation and Characterization of the Genes Causing Neurofibromatosis |
| Q34595912 | Random-breakage mapping method applied to human DNA sequences |
| Q67482160 | Rapid generation of region specific probes by chromosome microdissection and their application |
| Q36827610 | Ras p21: effects and regulation |
| Q35197416 | Refined physical and genetic mapping of the NF1 region on chromosome 17 |
| Q47753216 | SNTG1, the gene encoding gamma1-syntrophin: a candidate gene for idiopathic scoliosis |
| Q48447152 | Serum mitogenic activity on in vitro glial cells in Neurofibromatosis type 1. |
| Q35194587 | Tandem duplication within a neurofibromatosis type 1 (NF1) gene exon in a family with features of Watson syndrome and Noonan syndrome. |
| Q24324729 | The NF1 locus encodes a protein functionally related to mammalian GAP and yeast IRA proteins |
| Q54058558 | The Neurofibromatosis Type 1 (NF1) Gene: Identification and Partial Characterization of a Putative Tumor Suppressor Gene |
| Q24678711 | The neurofibroma in von Recklinghausen neurofibromatosis has a unicellular origin |
| Q28218535 | WAVE3, an actin-polymerization gene, is truncated and inactivated as a result of a constitutional t(1;13)(q21;q12) chromosome translocation in a patient with ganglioneuroblastoma |
| Q24317747 | cDNA sequence and genomic structure of EV12B, a gene lying within an intron of the neurofibromatosis type 1 gene |