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PMID: 2491781 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Close flanking markers for neurofibromatosis type I (NF1).

American journal of human genetics ·Vol. 44 ·No. 1 ·1989-01-00 ·页码 41-7

Upadhyaya M, Sarfarazi M, Huson SM, Broadhead W, Fryer A, Harper PS

Abstract

A genetic linkage study with 16 polymorphic DNA markers spanning the region 17p11-17q24 in 22 NF1 families is presented. Close linkage between NF1 and eight pericentromeric markers (HHH202, EW206, CRI-L946, EW203, EW301, FG2, p17H8, and CRI-L581) has been found, probe HHH202 being the closest marker to NF1. Genetic heterogeneity has been excluded. The study of multiply informative meioses suggests that the probes HHH202 and RW206 are flanking markers for NF1. The most likely order on the basis of multiply informative meioses and multipoint mapping is pter-pA10.41-EW301-cen-HHH202-NF1-EW206-++ +EW207-qter.

MeSH 主题词
Chromosome Mapping Chromosomes, Human, Pair 17 Female Genetic Linkage Genetic Markers Humans Male Neurofibromatosis 1/genetics Pedigree Recombination, Genetic
化学物质
Genetic Markers
作者与单位
共 6 位作者,点击展开单位 / ORCID
Upadhyaya M
Institute of Medical Genetics, University of Wales College of Medicine, Cardiff, United Kingdom.
Sarfarazi M
Huson S M
Broadhead W
Fryer A
Harper P S
Article Info
Journal
American journal of human genetics
Abbr.
Am J Hum Genet
ISSN
0002-9297
Published
1989-01-00
页码
41-7
Language
English
Country/Region
United States
NLM ID
0370475
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