(Q35644589)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7668262%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

title

Evidence that the ancestral haplotype in Australian hemochromatosis patients may be associated with a common mutation in the gene (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7668262%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

author name string

Crawford DH

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7668262%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

Powell LW

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7668262%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

Leggett BA

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7668262%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

Francis JS

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7668262%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

Fletcher LM

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7668262%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

Webb SI

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7668262%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

Halliday JW

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7668262%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

Jazwinska EC

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7668262%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

language of work or name

English

0 references

publication date

1 August 1995

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7668262%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

number of pages

6

1 reference

American Journal of Human Genetics

inferred from page(s)

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7668262%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

volume

57

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7668262%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7668262%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

page(s)

362-367

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7668262%20AND%20SRC:MED&resulttype=core&format=json

Localization of the hemochromatosis gene close to D6S105.

23 October 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801553

Mapping, cloning and genetic characterization of the region containing the Wilson disease gene.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801553

Haplotype analysis in Australian hemochromatosis patients: evidence for a predominant ancestral haplotype exclusively associated with hemochromatosis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801553

Evidence for heterogeneity in hereditary hemochromatosis. Evaluation of 174 persons in nine families

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801553

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801553

Factors affecting the concentrations of ferritin in serum in a healthy Australian population.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801553

Expression of hemochromatosis in homozygous subjects. Implications for early diagnosis and prevention

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801553

The relation between genotype and phenotype in cystic fibrosis--analysis of the most common mutation (delta F508).

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801553

Association of HLA-A3 and HLA-B14 antigens with idiopathic haemochromatosis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801553

Hereditary hemochromatosis. Diagnosis in siblings and children

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801553

Hereditary hemochromatosis. Phenotypic expression of the disease

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801553

Concordance of iron storage in siblings with genetic hemochromatosis: evidence for a predominantly genetic effect on iron storage

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801553

Mutations in CFTR associated with mild-disease-form Cl- channels with altered pore properties.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801553

The Wilson disease gene: spectrum of mutations and their consequences

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801553

Idiopathic haemochromatosis in the Australian population: HLA linkage and recessivity

25 September 2018

1 reference

12 December 2020

Value of hepatic iron measurements in early hemochromatosis and determination of the critical iron level associated with fibrosis

1 reference

12 December 2020

Identification of homozygous hemochromatosis subjects by measurement of hepatic iron index

1 reference

12 December 2020

Prevalence of abnormal iron studies in heterozygotes for hereditary hemochromatosis: an analysis of 255 heterozygotes

1 reference

12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7668262%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

PubMed publication ID

7668262

1 reference