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PMID: 2896629 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Linkage studies with chromosome 17 DNA markers in 45 neurofibromatosis 1 families.

Genomics ·Vol. 1 ·No. 4 ·1987-12-00 ·页码 353-7

Stephens K, Riccardi VM, Rising M, Ng S, Green P, Collins FS, Rediker KS, Powers JA, Parker C, Donis-Keller H

Abstract

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.

MeSH 主题词
Chromosomes, Human, Pair 17 DNA/analysis Female Genetic Linkage Genetic Markers Humans Lod Score Male Mutation Neurofibromatosis 1/genetics Polymorphism, Restriction Fragment Length Recombination, Genetic
化学物质
Genetic Markers DNA
作者与单位
共 10 位作者,点击展开单位 / ORCID
Stephens K
Department of Human Genetics, Collaborative Research, Inc., Bedford, Massachusetts 01730.
Riccardi V M
Rising M
Ng S
Green P
Collins F S
Rediker K S
Powers J A
Parker C
Donis-Keller H
Article Info
Journal
Genomics
Abbr.
Genomics
ISSN
0888-7543
Published
1987-12-00
页码
353-7
Language
English
Country/Region
United States
NLM ID
8800135
基金资助
NINDS NIH HHS · NS23410 · United States
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