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English
Should we genetically test everyone for haemochromatosis?
scientific article published on April 1999
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
479209
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10226930%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
title
Should we genetically test everyone for haemochromatosis?
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
479209
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10226930%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
author
Katie Allen
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
479209
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10226930%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
author name string
R Williamson
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
479209
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10226930%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
publication date
1 April 1999
1 reference
stated in
Europe PubMed Central
PMC publication ID
479209
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10226930%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
published in
Journal of Medical Ethics
1 reference
stated in
Europe PubMed Central
PMC publication ID
479209
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10226930%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
volume
25
1 reference
stated in
Europe PubMed Central
PMC publication ID
479209
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10226930%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
issue
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
479209
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10226930%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
page(s)
209-214
1 reference
stated in
Europe PubMed Central
PMC publication ID
479209
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10226930%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
cites work
Clinical and biochemical abnormalities in people heterozygous for hemochromatosis
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=479209
retrieved
30 September 2017
A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis
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=479209
retrieved
30 September 2017
Universal community carrier screening for cystic fibrosis?
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=479209
retrieved
30 September 2017
Distress in individuals facing predictive DNA testing for autosomal dominant late-onset disorders: comparing questionnaire results with in-depth interviews. Rotterdam/Leiden Genetics Workgroup
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=479209
retrieved
28 June 2018
Diagnosis and management of hemochromatosis
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=479209
retrieved
28 June 2018
Problems in genetic prediction for Huntington's disease
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=479209
retrieved
28 June 2018
Hemochromatosis: genetics helps to define a multifactorial disease.
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=479209
retrieved
5 September 2018
Hereditary hemochromatosis: gene discovery and its implications for population-based screening
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=479209
retrieved
5 September 2018
Haemochromatosis: diagnosis and management after the cloning of the HFE 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=479209
retrieved
5 September 2018
Expression of HLA-linked hemochromatosis in subjects homozygous or heterozygous for the C282Y mutation.
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=479209
retrieved
5 September 2018
Increased hepatic iron concentration in nonalcoholic steatohepatitis is associated with increased fibrosis.
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=479209
retrieved
5 September 2018
Patients' attitudes about autonomy and confidentiality in genetic testing for breast-ovarian cancer susceptibility.
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=479209
retrieved
5 September 2018
A candidate gene for hemochromatosis: frequency of the C282Y and H63D mutations.
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=479209
retrieved
5 September 2018
Genetic discrimination and health insurance: an urgent need for reform.
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=479209
retrieved
5 September 2018
Simple non-invasive method to obtain DNA for gene analysis
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10226930
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Prevalence of haemochromatosis amongst asymptomatic Australians
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10226930
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Cost-effectiveness of mammographic screening in Australia
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10226930
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Hemochromatosis: the impact of early diagnosis and therapy
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10226930
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Alcoholism in hereditary hemochromatosis revisited: prevalence and clinical consequences among homozygous siblings
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10226930
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Analysis of the cost of population screening for haemochromatosis using biochemical and genetic markers
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10226930
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Heterogeneity of hemochromatosis in Italy
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10226930
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JME.25.2.209
1 reference
stated in
Europe PubMed Central
PMC publication ID
479209
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10226930%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
PMC publication ID
479209
1 reference
stated in
Europe PubMed Central
PMC publication ID
479209
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10226930%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
PubMed publication ID
10226930
1 reference
stated in
Europe PubMed Central
PMC publication ID
479209
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10226930%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
ResearchGate publication ID
13071402
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