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Neurofibromatosis type 1 (NF1) is caused by a change in the NF1 gene, which is found on chromosome 17. Chromosome 17 spans about 83 million DNA building blocks (base pairs) and represents between 2.5 and 3 percent of the total DNA in cells. F S Collins , B A Ponder , B R Seizinger , and C J Epstein Division of Medical Genetics, University of Michigan Medical Center, Ann Arbor 48109-0618. This gene is located on chromosome number 17.
Just a thought *Edit I for the illegal part wrong from reading certain articles Some people have features of NF1 that are limited to only one part of their body.
The von Recklinghausen neurofibromatosis (NF1) gene has been localized to the pericentromeric region of chromosome 17. Neurofibromatosis type 1 (von Recklinghausen's NF1) is an autosomal dominant disease associated with an increased risk of benign and malignant neoplasia including malignant peripheral nerve sheath tumors (MPNSTs). Some people have features of NF1 that are limited to only one part of their body. In this study, we employed comparative genomic hybridization (CGH) to determine changes in the relative chromosome copy number in 24 patients with neurofibromas, including 12 … The extent of the missing genetic material, as delineated by a combination of cytogenetics, FISH and MLPA, was 0.6–2.5 Mb on 17p, and up to about 10 Mb on 17q. Chromosome 17q11.2 deletion syndrome, 1.4Mb ; VAN ASPEREN SYNDROME; Del(17)(q11); Chromosome 17q11.2 deletion syndrome, 1.4Mb ; VAN ASPEREN SYNDROME; Del(17)(q11); Neurofibromatosis type 1 microdeletion syndrome; Monosomy 17q11; NF1 microdeletion syndrome; 17q11 microdeletion syndrome See More
ring chromosome 17. In this report, we present a girl whose relatively mild phenotype (neurofibromatosis type 1 (NF1), mild dysmorphic features, mental retardation, and autism) prompted us to perform a cytogenetic examination. More than 150 members in six families were typed with probes including HHH202, D17Z1, EW203, EW206, EW207, EW301, pA10–41, D17S37, … Structural abnormalities of chromosome 17, and ring chromo-somes of 17 in particular, are rare. We have screened six multigenerational families with multiple, tightly linked markers to aid in mapping this region of the chromosome. On y trouve notamment le gène p53, gène suppresseur de tumeurs également appelé « Gardien du génome ». The NF1 gene was cloned from human chromosome 17 in 1990. And then people won’t have to go through this awful condition. Molecular Biology. Identifying genes on each chromosome is an active area of genetic research. Because researchers use different approaches to predict the number of genes on each chromosome, the estimated number of genes varies. Gènes localisés sur le chromosome 17. M. MacCollin, in Encyclopedia of the Neurological Sciences (Second Edition), 2014.