(Q39585577)

13 September 2017

Development of a multiplex ARMS test for mutations in the HFE gene associated with hereditary haemochromatosis (English)

1 reference

13 September 2017

Baty D

1

1 reference

13 September 2017

Terron Kwiatkowski A

2

1 reference

13 September 2017

Mechan D

3

1 reference

13 September 2017

Harris A

4

1 reference

13 September 2017

Pippard MJ

5

1 reference

13 September 2017

Goudie D

6

1 reference

13 September 2017

language of work or name

English

0 references

publication date

1 January 1998

1 reference

Journal of Clinical Pathology

13 September 2017

1 reference

13 September 2017

51

1 reference

13 September 2017

1

1 reference

13 September 2017

73-74

1 reference

Global prevalence of putative haemochromatosis mutations

13 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=500436

A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=500436

Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS)

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=500436

Development, multiplexing, and application of ARMS tests for common mutations in the CFTR gene

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=500436

Mutation analysis in hereditary hemochromatosis

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=500436

Haemochromatosis and HLA-H.

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=500436

Cystic fibrosis mutation analysis: Report from 22 U.K. regional genetics laboratories

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=500436

The polymerase chain reaction with sequence specific primers for the detection of the factor V mutation associated with activated protein C resistance

2 December 2018

1 reference

12 December 2020

Long-term survival in patients with hereditary hemochromatosis

1 reference

12 December 2020

Haemochromatosis and HLA-H

1 reference

12 December 2020

Increased frequency of the haemochromatosis Cys282Tyr mutation in sporadic porphyria cutanea tarda

1 reference

12 December 2020

Mutations in the MHC class I-like candidate gene for hemochromatosis in French patients

1 reference

12 December 2020

Identifiers

DOI

10.1136/JCP.51.1.73

1 reference

13 September 2017

1 reference

13 September 2017

PubMed publication ID

9577377

1 reference