A locus for von Recklinghausen neurofibromatosis (NF1) has recently been mapped near the chromosome 17 centromere. We have extended these linkage studies by genotyping 45 NF1 families with three DNA probes known to be linked to the chromosome 17 centromeric region. Of 34 families informative for NF1 and at least one of the three probes, 28 families show no recombinants with the disease gene. These data provide additional support for genetic homogeneity of NF1 and for a primary NF1 locus linked to the chromosome 17 centromere. Among the informative families were 7 families with apparent new NF1 mutations. Our data suggest that these mutations are probably at the chromosome 17 NF1 locus.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/202...
Dans la famille étudiée les résultats excluent entre 20 à 30% du chromosome 8 comme localisation pos...
Neurofibromatosis type 1 (NF1) is a common autosomal dominant disorder characterized by multiple neu...
We report on a rare patient screened as a putative carrier of a contiguous gene syndrome on the basi...
Several recent studies indicate that the von Recklinghausen neurofibromatosis (NF1) gene is located ...
Von Recklinghausen neurofibromatosis (NF1) is a common autosomal dominant disorder of humans. Linkag...
Von Recklinghausen neurofibromatosis (NF1) is a common autosomal dominant disorder in all human popu...
Von Recklinghausen peripheral neurofibromatosis ( NF- 1 ), one of the most frequent , ubiquitous , c...
The authors report the results of a genetic analysis performed in 34 neurofibromatosis type 1 (NF1) ...
To establish preclinical DNA-diagnosis of neurofibromatosis type 1 (NF1) in familial cases we have i...
Von Recklinghausen neurofibromatosis or type l neurofibromatosis (NF1), is one of the most common au...
A somatic cell hybrid mapping panel was constructed to localize cloned DNA sequences to any of 15 po...
Neurofibromatosis type 1 (NF1) is a frequent hereditary disorder. The disease is characterized by a ...
Von Recklinghausen neurofibromatosis, or type 1 neurofibromatosis (NF1), is a common autosomal domin...
Homologous recombination between poorly characterized regions flanking the NF1 locus causes the cons...
Neurofibromatosis type 1 (NF1), formerly known as Von Recklinghausen Neurofibromatosis, is a common ...
Dans la famille étudiée les résultats excluent entre 20 à 30% du chromosome 8 comme localisation pos...
Neurofibromatosis type 1 (NF1) is a common autosomal dominant disorder characterized by multiple neu...
We report on a rare patient screened as a putative carrier of a contiguous gene syndrome on the basi...
Several recent studies indicate that the von Recklinghausen neurofibromatosis (NF1) gene is located ...
Von Recklinghausen neurofibromatosis (NF1) is a common autosomal dominant disorder of humans. Linkag...
Von Recklinghausen neurofibromatosis (NF1) is a common autosomal dominant disorder in all human popu...
Von Recklinghausen peripheral neurofibromatosis ( NF- 1 ), one of the most frequent , ubiquitous , c...
The authors report the results of a genetic analysis performed in 34 neurofibromatosis type 1 (NF1) ...
To establish preclinical DNA-diagnosis of neurofibromatosis type 1 (NF1) in familial cases we have i...
Von Recklinghausen neurofibromatosis or type l neurofibromatosis (NF1), is one of the most common au...
A somatic cell hybrid mapping panel was constructed to localize cloned DNA sequences to any of 15 po...
Neurofibromatosis type 1 (NF1) is a frequent hereditary disorder. The disease is characterized by a ...
Von Recklinghausen neurofibromatosis, or type 1 neurofibromatosis (NF1), is a common autosomal domin...
Homologous recombination between poorly characterized regions flanking the NF1 locus causes the cons...
Neurofibromatosis type 1 (NF1), formerly known as Von Recklinghausen Neurofibromatosis, is a common ...
Dans la famille étudiée les résultats excluent entre 20 à 30% du chromosome 8 comme localisation pos...
Neurofibromatosis type 1 (NF1) is a common autosomal dominant disorder characterized by multiple neu...
We report on a rare patient screened as a putative carrier of a contiguous gene syndrome on the basi...