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Risk reversals in predictive testing for Huntington disease.
scientific article
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
1715985
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382108%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
title
Risk reversals in predictive testing for Huntington disease
(English)
1 reference
stated in
Europe PubMed Central
PMCID
1715985
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382108%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
main subject
Huntington's disease
0 references
author
Shelin Adam
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
1715985
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382108%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
Michael R. Hayden
series ordinal
10
1 reference
stated in
Europe PubMed Central
PMCID
1715985
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382108%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
author name string
Almqvist E
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
1715985
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382108%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
Bloch M
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMCID
1715985
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382108%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
Fuller A
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMCID
1715985
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382108%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
Welch P
series ordinal
5
1 reference
stated in
Europe PubMed Central
PMCID
1715985
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382108%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
Eisenberg D
series ordinal
6
1 reference
stated in
Europe PubMed Central
PMCID
1715985
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382108%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
Whelan D
series ordinal
7
1 reference
stated in
Europe PubMed Central
PMCID
1715985
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382108%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
Macgregor D
series ordinal
8
1 reference
stated in
Europe PubMed Central
PMCID
1715985
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382108%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
Meschino W
series ordinal
9
1 reference
stated in
Europe PubMed Central
PMCID
1715985
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382108%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
language of work or name
English
0 references
publication date
1 October 1997
1 reference
stated in
Europe PubMed Central
PMCID
1715985
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382108%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
published in
American Journal of Human Genetics
1 reference
stated in
Europe PubMed Central
PMCID
1715985
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382108%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
volume
61
1 reference
stated in
Europe PubMed Central
PMCID
1715985
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382108%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
issue
4
1 reference
stated in
Europe PubMed Central
PMCID
1715985
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382108%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
page(s)
945-952
1 reference
stated in
Europe PubMed Central
PMCID
1715985
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382108%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
cites work
The likelihood of being affected with Huntington disease by a particular age, for a specific CAG size
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=1715985
retrieved
12 July 2018
Contribution of DNA sequence and CAG size to mutation frequencies of intermediate alleles for Huntington disease: evidence from single sperm analyses
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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=1715985
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12 July 2018
Hereditary breast and ovarian cancer: epidemiology, genetics, screening and predictive testing.
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12 July 2018
Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeats
1 reference
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PubMed Central
reference URL
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12 July 2018
Increased instability of intermediate alleles in families with sporadic Huntington disease compared to similar sized intermediate alleles in the general population
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PubMed Central
reference URL
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12 July 2018
A worldwide study of the Huntington's disease mutation. The sensitivity and specificity of measuring CAG repeats
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12 July 2018
Sex-dependent mechanisms for expansions and contractions of the CAG repeat on affected Huntington disease chromosomes
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=1715985
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12 July 2018
Genetic aspects of multiple endocrine neoplasia types 1 and 2.
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12 July 2018
A polymorphic DNA marker genetically linked to Huntington's disease
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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=1715985
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12 July 2018
Presymptomatic testing for Huntington's disease
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=1715985
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12 July 2018
Improved predictive testing for Huntington disease by using three linked DNA markers
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PubMed Central
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12 July 2018
Psychiatric implications of presymptomatic testing for Huntington's disease
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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=1715985
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12 July 2018
Presymptomatic testing for Huntington chorea: guidelines for moral and social accountability
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715985
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12 July 2018
Ethics of predictive testing for Huntington's chorea: the need for more information
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715985
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12 July 2018
Suicide and attempted suicide in Huntington disease: implications for preclinical testing of persons at risk
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PubMed Central
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12 July 2018
A highly polymorphic locus very tightly linked to the Huntington's disease gene
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715985
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12 July 2018
A DNA segment encoding two genes very tightly linked to Huntington's disease
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715985
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12 July 2018
Predictive testing for Huntington disease: II. Demographic characteristics, life-style patterns, attitudes, and psychosocial assessments of the first fifty-one test candidates
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12 July 2018
Predictive testing for Huntington disease: I. Description of a pilot project in British Columbia
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12 July 2018
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12 July 2018
Predictive testing for Huntington disease in Canada: adverse effects and unexpected results in those receiving a decreased risk
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715985
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12 July 2018
Predictive testing for Huntington disease in Canada: the experience of those receiving an increased risk
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=1715985
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12 July 2018
A PCR method for accurate assessment of trinucleotide repeat expansion in Huntington disease
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=1715985
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26 September 2018
Refinement by linkage analysis in two large families of the candidate region of the third locus (SCA3) for autosomal dominant cerebellar ataxia type I
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9382108
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1086/514873
1 reference
stated in
Europe PubMed Central
PMCID
1715985
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382108%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
PMCID
1715985
1 reference
stated in
Europe PubMed Central
PMCID
1715985
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382108%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
PubMed ID
9382108
1 reference
stated in
Europe PubMed Central
PMCID
1715985
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9382108%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
ResearchGate publication ID
13848103
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