(Q40839656)

24 September 2017

1 reference

title

Genetics of common disease: implications for therapy, screening and redefinition of disease (English)

1 reference

24 September 2017

Bell J

1

1 reference

PMC publication ID

1691990

24 September 2017

language of work or name

English

0 references

publication date

1 August 1997

1 reference

Philosophical Transactions of the Royal Society B

24 September 2017

1 reference

24 September 2017

352

1 reference

24 September 2017

1357

1 reference

24 September 2017

1051-1055

1 reference

Lessons from hereditary colorectal cancer

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1691990

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

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1691990

BRCA1 is secreted and exhibits properties of a granin

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1691990

Identification of the breast cancer susceptibility gene BRCA2

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1691990

Familial hyperglycemia due to mutations in glucokinase. Definition of a subtype of diabetes mellitus

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1691990

A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1691990

HLA heterozygosity contributes to susceptibility to rheumatoid arthritis

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1691990

Apolipoprotein E genotyping in the differential diagnosis, not prediction, of Alzheimer's disease

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1691990

Deletion polymorphism in the gene for angiotensin-converting enzyme is a potent risk factor for myocardial infarction

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1691990

Two stage genome-wide search in inflammatory bowel disease provides evidence for susceptibility loci on chromosomes 3, 7 and 12

2 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9304670

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1098/RSTB.1997.0084

1 reference

24 September 2017

1 reference

PMC publication ID

1691990

24 September 2017

PubMed publication ID

9304670

1 reference

PMC publication ID

1691990