Evidence map›Paper›PMID 1570832›Full record

ArticleAmerican journal of human genetics1992

Band-specific localization of the microsatellite at D13S71 by microdissection and enzymatic amplification.

H Spielvogel, H C Hennies, U Claussen, S S Washington, A Chakravarti, A Reis

Abstract read
In one paragraph

Article in American journal of human genetics, 1992. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

H SpielvogelInstitut für Humangenetik Universität, Erlangen, Germany.
H C Hennies
U Claussen
S S Washington
A Chakravarti
A Reis

Funding

Genetic Analysis of Hirschsprung Disease - RenewalR01HD028088 · NICHD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CHAKRAVARTI, ARAVINDA · 1991 to 2024
$6.2M
NICHD NIH HHS HD28088
6 · The paper itself

Abstract

Microsatellite DNA consists of tandemly repeated simple DNA sequence motifs, the number of these repeats being polymorphic. These recently described polymorphisms are ubiquitously distributed throughout the human genome and are highly informative, making them ideal markers for linkage analysis. Physical localization of these microsatellites is an important prerequisite for aligning physical and genetic maps. We have physically mapped the microsatellite at D13S71, which has previously been assigned to chromosome 13. Band-specific mapping of D13S71 to the distal part of band 13q32, near 13q33, was achieved by microdissection of GTG-banded chromosomes and subsequent enzymatic amplification with a heminested PCR approach. Analysis of a panel of somatic cell hybrids confirmed this localization. The technique presented may also be useful in a variety of complex mapping situations and whenever the precise localization of very small (as small as 70 bp) DNA probes is necessary.

Indexed as

Chromosomes, Human, Pair 13Base SequenceChromosome MappingDNA, SatelliteHumansHybrid CellsMolecular Sequence DataPolymerase Chain ReactionPolymorphism, GeneticRepetitive Sequences, Nucleic AcidDNA, Satellite

Identifiers

PMID1570832
PMCPMC1682594

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.