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The Human Gene Mutation Database. at the Institute of Medical Genetics in Cardiff Research - Neurofibromatosis Network Neurofibromatosis Research Program Announcements. The NF Network plays a vital role in securing federal funds for Neurofibromatosis Research. One of the federal programs funded is the Congressionally Directed Medical Research Program, specifically the Neurofibromatosis Research Program Check out the NF Research Program Announcements for 2019. NF1 gene homepage - Global Variome shared LOVD Graphical displays and utilities; Graphs: Graphs displaying summary information of all variants in the database »: Reading frame checker: The Reading-frame checker generates a prediction of the effect of whole-exon changes. Seizures occur in people with Neurofibromatosis type 1

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OMIM Entry - * 613113 - NEUROFIBROMIN 1; NF1

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Neurofibromatosis Type 1 | Children's Hospital of Philadelphia

News Stories Archive - Neurofibromatosis (NF) Center New Study Finds Deficits in Adaptive Functioning are Common in Children with NF1. Most children with Neurofibromatosis Type 1 (NF1) have difficulties with learning and/or behavior; however, these problems vary significantly between individuals. Skin, Bone and Eye Abnormalities - Neurofibromatosis (NF Skin, Bone and Eye Abnormalities. Most individuals with NF1 have multiple café-au-lait macules and/or skinfold freckling. Individuals with NF1 are also more prone to developing bone and eye abnormalities.