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A Comprehensive Genetic Linkage Map of the Human Genome

NIH/CEPH Collaborative Mapping Group·1992·Science

Abstract

A genetic linkage map of the human genome was constructed that consists of 1416 loci, including 279 genes and expressed sequences. The loci are represented by 1676 polymorphic systems genotyped with the CEPH reference pedigree resource. A total of 339 microsatellite repeat markers assayed by PCR are contained within the map, and of the 351 markers with heterozygosities of at least 70%, 205 are microsatellites. Seven telomere loci define physical and genetic endpoints for 2q, 4p, 7q, 8p, 14q, 16p, and 16q, and in other cases distal markers on the maps have been localized to terminal cytogenetic bands. Therefore, at least 92% of the autosomal length of the genome and 95% of the X chromosome is estimated to be spanned by the map. Since the maps have relatively high marker density and numerous highly informative loci, they can be used to map disease phenotypes, even for those with limited pedigree resources. The baseline map provides a foundation for achieving continuity of clone-based physical maps and for the development of a truly integrated physical, genetic, and cytogenetic map of the human.

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Metadata

Authors
NIH/CEPH Collaborative Mapping Group
Venue
Science
Published
1992-10-02
Volume
258
Issue
5079
Pages
67-86
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W4211252102
Cited by
358
References
6
FWCI
45.01
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: A Comprehensive Genetic Linkage Map of the Human Genome. https://app.cochat.ai/papers/10.1126/science.1439770
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NIH/CEPH Collaborative Mapping Group. (1992). A Comprehensive Genetic Linkage Map of the Human Genome. Science. https://doi.org/10.1126/science.1439770

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