(Q42850818)

8 November 2017

Homogeneous multiplex genotyping of hemochromatosis mutations with fluorescent hybridization probes (English)

1 reference

8 November 2017

1 reference

P S Bernard

1

1 reference

8 November 2017

R S Ajioka

series ordinal

2

1 reference

8 November 2017

J P Kushner

series ordinal

3

1 reference

8 November 2017

C T Wittwer

series ordinal

4

1 reference

8 November 2017

language of work or name

English

0 references

publication date

1 October 1998

1 reference

The American Journal of Pathology

8 November 2017

1 reference

8 November 2017

153

1 reference

8 November 2017

4

1 reference

8 November 2017

1055-1061

1 reference

Screening for hemochromatosis: phenotype versus genotype

8 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853057

Seven-color time-resolved fluorescence hybridization analysis of human papilloma virus types

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853057

Multiplex systems for the amplification of short tandem repeat loci: evaluation of laser fluorescence detection

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853057

Haplotype analysis of hemochromatosis: evaluation of different linkage-disequilibrium approaches and evolution of disease chromosomes

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853057

Mutation analysis of the HLA-H gene in Italian hemochromatosis patients

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853057

Mutation analysis in hereditary hemochromatosis

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853057

Haemochromatosis and HLA-H.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853057

Database of mutations in the p53 and APC tumor suppressor genes designed to facilitate molecular epidemiological analyses

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853057

Multiplex, fluorescent, solid-phase minisequencing for efficient screening of DNA sequence variation.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853057

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

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853057

Influence of nearest neighbor sequence on the stability of base pair mismatches in long DNA; determination by temperature-gradient gel electrophoresis

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853057

Hereditary hemochromatosis. Analysis of laboratory expression of the disease by genotype in 18 pedigrees

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853057

Hereditary haemochromatosis.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853057

Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853057

DNA extraction with organic solvents in gel barrier tubes.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853057

DNA probes: applications of the principles of nucleic acid hybridization

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853057

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

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853057

A candidate gene for hemochromatosis: frequency of the C282Y and H63D mutations.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853057

The significance of the 187G (H63D) mutation in hemochromatosis

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853057

Prevalence of heterozygotes for hemochromatosis in the white population of the United States.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853057

A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC)

16 August 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965650-7

Idiopathic hemochromatosis. Demonstration of recessive transmission and early detection by family HLA typing

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965650-7

Prevalence of Hemochromatosis among 11,065 Presumably Healthy Blood Donors

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965650-7

Integrated amplification and detection of the C677T point mutation in the methylenetetrahydrofolate reductase gene by fluorescence resonance energy transfer and probe melting curves

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965650-7

Continuous fluorescence monitoring of rapid cycle DNA amplification

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965650-7

Enhanced discrimination of single nucleotide polymorphisms by artificial mismatch hybridization

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965650-7

An evaluation of selected DNA extraction strategies for short tandem repeat typing

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965650-7

Analysis of the cost of population screening for haemochromatosis using biochemical and genetic markers

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965650-7

Hemosiderosis in cirrhosis: a study of 447 native livers

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965650-7

Towards fully automated genome-wide polymorphism screening

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965650-7

Molecular beacon sequence analysis for detecting drug resistance in Mycobacterium tuberculosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965650-7

Simultaneous detection of multiple point mutations using fluorescence-coupled competitive primer extension

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965650-7

Multiplex PCR: critical parameters and step-by-step protocol

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965650-7

HLA-H mutations in the Ashkenazi Jewish population

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965650-7

Real-time fluorescence genotyping of factor V Leiden during rapid-cycle PCR

7 January 2021

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9777937

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genetic testing for cystic fibrosis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9777937

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A cheaper and more rapid polymerase chain reaction-restriction fragment length polymorphism method for the detection of the HLA-H gene mutations occurring in hereditary hemochromatosis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9777937

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/S0002-9440(10)65650-7

1 reference

8 November 2017

1 reference

8 November 2017

PubMed publication ID

9777937

1 reference