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PMID: 2491775 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Genetic analysis of eight loci tightly linked to neurofibromatosis 1.

American journal of human genetics ·Vol. 44 ·No. 1 ·1989-01-00 ·Pages 13-9

Stephens K, Green P, Riccardi VM, Ng S, Rising M, Barker D, Darby JK, Falls KM, Collins FS, Willard HF

Abstract

The genetic locus for neurofibromatosis 1 (NF1) has recently been mapped to the pericentromeric region of chromosome 17. We have genotyped eight previously identified RFLP probes on 50 NF1 families to determine the placement of the NF1 locus relative to the RFLP loci. Thirty-eight recombination events in the pericentromeric region were identified, eight involving crossovers between NF1 and loci on either chromosomal arm. Multipoint linkage analysis resulted in the unique placement of six loci at odds greater than 100:1 in the order of pter-A10-41-EW301-NF1-EW207-CRI-L581-CRI-L946 -qter. Owing to insufficient crossovers, three loci--D17Z1, EW206, and EW203--could not be uniquely localized. In this region female recombination rates were significantly higher than those of males. These data were part of a joint study aimed at the localization of both NF1 and tightly linked pericentromeric markers for chromosome 17.

MeSH Terms
Chromosome Mapping Chromosomes, Human, Pair 17 Genetic Linkage Genetic Markers Humans Neurofibromatosis 1/genetics Recombination, Genetic
Chemicals
Genetic Markers
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Stephens K
Department of Human Genetics, Collaborative Research, Inc., Bedford, MA 01730.
Green P
Riccardi V M
Ng S
Rising M
Barker D
Darby J K
Falls K M
Collins F S
Willard H F
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Article Info
Journal
American journal of human genetics
Abbr.
Am J Hum Genet
ISSN
0002-9297
Published
1989-01-00
Pages
13-9
Language
English
Region
United States
NLM ID
0370475
PMCID
PMC1715471
Subset
IM
Grants
DS NIH HHS · NINCDS 22936 · United States
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