(Q35197657)

7 August 2017

title

Exclusion of the retinoblastoma gene and chromosome 13q as the site of a primary lesion for human breast cancer (English)

1 reference

7 August 2017

1 reference

A M Bowcock

1

1 reference

7 August 2017

J M Hall

series ordinal

2

1 reference

7 August 2017

J M Hebert

series ordinal

3

1 reference

7 August 2017

M C King

series ordinal

4

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 January 1990

1 reference

American Journal of Human Genetics

7 August 2017

published in

1 reference

7 August 2017

volume

46

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7 August 2017

issue

1

1 reference

7 August 2017

page(s)

12-17

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A systematic approach for detecting high-frequency restriction fragment length polymorphisms using large genomic probes

7 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683535

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683535

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683535

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683535

A primary genetic map of chromosome 13q.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683535

Inactivation of the retinoblastoma susceptibility gene in human breast cancers

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683535

Inheritance of human breast cancer: evidence for autosomal dominant transmission in high-risk families

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683535

Eight closely linked loci place the Wilson disease locus within 13q14-q21.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683535

Localization of the gene for familial adenomatous polyposis on chromosome 5.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683535

Loss of heterozygosity in human ductal breast tumors indicates a recessive mutation on chromosome 13

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683535

Localization of the genetic defect in familial adenomatous polyposis within a small region of chromosome 5

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683535

High recombination between two physically close human basement membrane collagen genes at the distal end of chromosome 13q.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683535

Human retinoblastoma susceptibility gene: genomic organization and analysis of heterozygous intragenic deletion mutants

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683535

Clonal analysis of human colorectal tumors

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683535

Chromosome 5 allele loss in human colorectal carcinomas.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683535

A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683535

A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683535

Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683535

Allelotype of colorectal carcinomas

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683535

Oncogenes and human breast cancer

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683535

Detection of high incidence of K-ras oncogenes during human colon tumorigenesis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683535

Rare HRAS alleles and susceptibility to human breast cancer

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683535

The gene for familial polyposis coli maps to the long arm of chromosome 5.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683535

Loss of constitutional heterozygosity in colon carcinoma from patients with familial polyposis coli.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683535

Deletion of genes on chromosome 1 in endocrine neoplasia

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683535

Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage

8 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683535

Prediction of the Risk of Hereditary Retinoblastoma, Using DNA Polymorphisms within the Retinoblastoma Gene

8 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2294744

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Lack of linkage of familial Wilms' tumour to chromosomal band 11 p13

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2294744

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Prevalence of ras gene mutations in human colorectal cancers

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2294744

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

PMC publication ID

1683535

1 reference

7 August 2017

1 reference