(Q35197191)

English

Linkage analysis of families with hereditary retinoblastoma: nonpenetrance of mutation, revealed by combined use of markers within and flanking the RB1 gene

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scholarly article

1 reference

Europe PubMed Central

7 August 2017

Linkage analysis of families with hereditary retinoblastoma: nonpenetrance of mutation, revealed by combined use of markers within and flanking the RB1 gene (English)

1 reference

Europe PubMed Central

7 August 2017

1 reference

based on heuristic

inferred from title

author name string

Scheffer H

1

1 reference

Europe PubMed Central

7 August 2017

te Meerman GJ

2

1 reference

Europe PubMed Central

7 August 2017

Kruize YC

3

1 reference

Europe PubMed Central

7 August 2017

van den Berg AH

4

1 reference

Europe PubMed Central

7 August 2017

Penninga DP

5

1 reference

Europe PubMed Central

7 August 2017

Tan KE

6

1 reference

Europe PubMed Central

7 August 2017

der Kinderen DJ

7

1 reference

Europe PubMed Central

7 August 2017

Buys CH

8

1 reference

Europe PubMed Central

7 August 2017

language of work or name

0 references

publication date

1 August 1989

1 reference

Europe PubMed Central

7 August 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

7 August 2017

45

1 reference

Europe PubMed Central

7 August 2017

252-260

1 reference

Europe PubMed Central

7 August 2017

2

1 reference

Europe PubMed Central

7 August 2017

Retinoma: spontaneous regression of retinoblastoma or benign manifestation of the mutation?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683338

13 July 2018

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683338

13 July 2018

Easy calculations of lod scores and genetic risks on small computers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683338

13 July 2018

Genomic sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683338

13 July 2018

Isolation and regional localization of DNA segments revealing polymorphic loci from human chromosome 13

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683338

13 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683338

13 July 2018

Isolation of human chromosome 13-specific DNA sequences cloned from flow sorted chromosomes and potentially linked to the retinoblastoma locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683338

13 July 2018

The practical management of retinoblastoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683338

13 July 2018

Mutation and cancer: statistical study of retinoblastoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683338

13 July 2018

An anonymous single copy genomic clone at 13q12-13q13 identifies three RFLPs [HGM8 assignment no. D13S11].

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683338

13 July 2018

Human retinoblastoma susceptibility gene: cloning, identification, and sequence.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683338

13 July 2018

Separation of large DNA molecules by contour-clamped homogeneous electric fields

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683338

13 July 2018

Cloning of the esterase D gene: a polymorphic gene probe closely linked to the retinoblastoma locus on chromosome 13

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683338

13 July 2018

Molecular evidence that the esterase-D gene lies proximal to the retinoblastoma susceptibility locus in chromosome region 13q14.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683338

13 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683338

13 July 2018

Identification of germline and somatic mutations affecting the retinoblastoma gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683338

13 July 2018

Sequences homologous to the human D1S1 locus present on human chromosome 3.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683338

13 July 2018

Structural evidence for the authenticity of the human retinoblastoma gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683338

13 July 2018

A straightforward approach to isolate DNA sequences with potential linkage to the retinoblastoma locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683338

13 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683338

13 July 2018

Familial, EsD-linked, retinoblastoma with reduced penetrance and variable expressivity.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683338

26 September 2018

Regional assignment of genes for human esterase D and retinoblastoma to chromosome band 13q14

1 reference

https://pubmed.ncbi.nlm.nih.gov/2569269

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygosity of chromosome 13 in retinoblastoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/2569269

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic analysis of retinoblastoma: evidence for multifocal origin and in vivo gene amplification

1 reference

https://pubmed.ncbi.nlm.nih.gov/2569269

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic forms of retinoblastoma: their incidence in a survey of 66 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/2569269

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Early diagnosis in hereditary retinoblastoma by detection of molecular deletions at gene locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/2569269

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2569269

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary retinoblastoma: penetrance, expressivity and age of onset

1 reference

https://pubmed.ncbi.nlm.nih.gov/2569269

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetics of retinoblastoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/2569269

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

7 August 2017

1 reference

Europe PubMed Central

7 August 2017

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