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Influence of aberrant observations on high-resolution linkage analysis outcomes
scientific article
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
1928104
retrieved
7 August 2017
title
Influence of aberrant observations on high-resolution linkage analysis outcomes
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
1928104
retrieved
7 August 2017
author name string
K H Buetow
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
1928104
retrieved
7 August 2017
language of work or name
English
0 references
publication date
1 November 1991
1 reference
stated in
Europe PubMed Central
PubMed ID
1928104
retrieved
7 August 2017
published in
American Journal of Human Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
1928104
retrieved
7 August 2017
volume
49
1 reference
stated in
Europe PubMed Central
PubMed ID
1928104
retrieved
7 August 2017
issue
5
1 reference
stated in
Europe PubMed Central
PubMed ID
1928104
retrieved
7 August 2017
page(s)
985-994
1 reference
stated in
Europe PubMed Central
PubMed ID
1928104
retrieved
7 August 2017
cites work
Strategies for multilocus linkage analysis in humans
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683261
retrieved
13 July 2018
Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683261
retrieved
13 July 2018
Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683261
retrieved
13 July 2018
A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683261
retrieved
13 July 2018
MAP, an expert system for multiple pairwise linkage analysis.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683261
retrieved
13 July 2018
Recombination events suggest potential sites for the Huntington's disease gene
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683261
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13 July 2018
Identification of the cystic fibrosis gene: genetic analysis
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683261
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13 July 2018
Cloning the gene for an inherited human disorder--chronic granulomatous disease--on the basis of its chromosomal location
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683261
retrieved
13 July 2018
Molecular history of gene conversions in the primate fetal gamma-globin genes. Nucleotide sequences from the common gibbon, Hylobates lar.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683261
retrieved
13 July 2018
Standard maps of chromosome 10.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683261
retrieved
13 July 2018
Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683261
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13 July 2018
The CEPH consortium linkage map of human chromosome 1
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683261
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13 July 2018
Gene conversion in steroid 21-hydroxylase genes.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683261
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13 July 2018
Extent and high frequency of a short conversion between the human A? and G? fetal globin genes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683261
retrieved
13 July 2018
A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination rates
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683261
retrieved
13 July 2018
Linkage analysis with misclassification at one locus.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683261
retrieved
13 July 2018
An initiation site for meiotic gene conversion in the yeast Saccharomyces cerevisiae
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/1928104
retrieved
12 December 2020
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Identifiers
PMCID
1683261
1 reference
stated in
Europe PubMed Central
PubMed ID
1928104
retrieved
7 August 2017
PubMed ID
1928104
1 reference
stated in
Europe PubMed Central
PubMed ID
1928104
retrieved
7 August 2017
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