The sequence of five non-contiguous genomic fragments encompassing 14.4 kilobases from the NF1 locus have been determined by fluorescence-based automated DNA sequence analysis. These fragments included one kilobase of the NF1 coding region, which resulted in the identification of the intron/exon boundaries of five exons. Based on these sequences, five new NF1 exon-PCR assays have been developed, that could be useful for detecting new NF1 mutations. The genomic sequences were analyzed for the presence of Alu repetitive elements and their classification is described. This analysis may provide some insight into the characterization of genetic rearrangements resulting in disruption of the NF1 gene
The high mutation rate at the NF1 locus results in a wide range of molecular abnormalities. The majo...
NF1 microdeletion syndrome is caused by haploinsufficiency of the NF1 gene and its flanking regions....
Neurofibromatosis Type I (NF1) is a multi systemic autosomal dominant neurocutaneous disorder predis...
Neurofibromatosis 1 (NF1) is one of the most common genetic disorders and is caused by mutations in ...
Neurofibromatosis type 1 (NF1) is a common autosomal dominant disease caused by various types of mut...
PURPOSE: To analyze the spectrum and frequency of NF1 mutations in exon 10b. METHODS: Mutation and s...
Long interspersed (L1) and Alu elements are actively amplified in the human genome through retrotran...
Neurofibromatosis type 1 (NF1) is a common autosomal dominant disorder characterized by a marked var...
A neurofibromatosis type I (NF1)-related locus has been identified on chromosome 15. It contains a p...
Numerous NF1 pseudogenes have been identified in the human genome. Those in 2q21, 14q11, and 22q11 f...
BACKGROUND: Segmental duplications flanking the neurofibromatosis type 1 (NF1) gene locus on 17q11...
Neurofibromatosis type 1 (NF1), one of the most common autosomal dominant disorders, is caused by mu...
To estimate the contribution of single and multi-exon NF1 gene copy-number changes to the NF1 mutati...
The high mutation rate at the NF1 locus results in a wide range of molecular abnormalities. The majo...
In a recent study we have documented by high resolution FISH the duplication of NF1 gene and several...
The high mutation rate at the NF1 locus results in a wide range of molecular abnormalities. The majo...
NF1 microdeletion syndrome is caused by haploinsufficiency of the NF1 gene and its flanking regions....
Neurofibromatosis Type I (NF1) is a multi systemic autosomal dominant neurocutaneous disorder predis...
Neurofibromatosis 1 (NF1) is one of the most common genetic disorders and is caused by mutations in ...
Neurofibromatosis type 1 (NF1) is a common autosomal dominant disease caused by various types of mut...
PURPOSE: To analyze the spectrum and frequency of NF1 mutations in exon 10b. METHODS: Mutation and s...
Long interspersed (L1) and Alu elements are actively amplified in the human genome through retrotran...
Neurofibromatosis type 1 (NF1) is a common autosomal dominant disorder characterized by a marked var...
A neurofibromatosis type I (NF1)-related locus has been identified on chromosome 15. It contains a p...
Numerous NF1 pseudogenes have been identified in the human genome. Those in 2q21, 14q11, and 22q11 f...
BACKGROUND: Segmental duplications flanking the neurofibromatosis type 1 (NF1) gene locus on 17q11...
Neurofibromatosis type 1 (NF1), one of the most common autosomal dominant disorders, is caused by mu...
To estimate the contribution of single and multi-exon NF1 gene copy-number changes to the NF1 mutati...
The high mutation rate at the NF1 locus results in a wide range of molecular abnormalities. The majo...
In a recent study we have documented by high resolution FISH the duplication of NF1 gene and several...
The high mutation rate at the NF1 locus results in a wide range of molecular abnormalities. The majo...
NF1 microdeletion syndrome is caused by haploinsufficiency of the NF1 gene and its flanking regions....
Neurofibromatosis Type I (NF1) is a multi systemic autosomal dominant neurocutaneous disorder predis...