(Q35993026)

English

Follow-up of retinoblastoma patients having prenatal and perinatal predictions for mutant gene carrier status using intragenic polymorphic probes from the RB1 gene

scientific article published on May 1, 1992

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scholarly article

1 reference

Europe PubMed Central

11 August 2017

Follow-up of retinoblastoma patients having prenatal and perinatal predictions for mutant gene carrier status using intragenic polymorphic probes from the RB1 gene (English)

1 reference

Europe PubMed Central

11 August 2017

1 reference

based on heuristic

inferred from title

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1350208

17 September 2022

author name string

Z. Onadim

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1350208

17 September 2022

J. Hungerford

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1350208

17 September 2022

J. K. Cowell

3

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1350208

17 September 2022

language of work or name

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publication date

1 May 1992

1 reference

Europe PubMed Central

11 August 2017

full work available at URL

https://europepmc.org/articles/PMC1977377

online access status

content deliverer

Europe PubMed Central

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1350208

17 September 2022

https://europepmc.org/articles/PMC1977377?pdf=render

Portable Document Format

online access status

content deliverer

Europe PubMed Central

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1350208

17 September 2022

British Journal of Cancer

1 reference

Europe PubMed Central

11 August 2017

65

1 reference

Europe PubMed Central

11 August 2017

711-716

1 reference

Europe PubMed Central

11 August 2017

5

1 reference

Europe PubMed Central

11 August 2017

https://scigraph.springernature.com/pub.10.1038/bjc.1992.150

0 references

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=1977377

2 October 2017

Deletions of a DNA sequence in retinoblastomas and mesenchymal tumors: organization of the sequence and its encoded protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1977377

2 October 2017

Deletion (13)(q14.1q14.3) in two generations: variability of ocular manifestations and definition of the phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1977377

2 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1977377

2 October 2017

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=1977377

2 October 2017

Structure and partial genomic sequence of the human retinoblastoma susceptibility gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1977377

2 October 2017

Mutations in the RB1 gene and their effects on transcription

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1977377

2 October 2017

Detection of DNA sequence polymorphisms by enzymatic amplification and direct genomic sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1977377

2 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1977377

2 October 2017

PCR-based detection of a polymorphic BamHI site in intron 1 of the human retinoblastoma (RB) gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1977377

2 October 2017

Carrier detection and prenatal screening of the retinoblastoma gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1977377

2 October 2017

Genetic counselling in retinoblastoma: importance of ocular fundus examination of first degree relatives and linkage analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1977377

2 October 2017

Application of intragenic DNA probes in prenatal screening for retinoblastoma gene carriers in the United Kingdom.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1977377

2 October 2017

Detection of the XbaI RFLP within the retinoblastoma locus by PCR.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1977377

2 October 2017

Application of PCR amplification of DNA from paraffin embedded tissue sections to linkage analysis in familial retinoblastoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1977377

2 October 2017

Genetic and cytogenetic analysis of patients showing reduced esterase-D levels and mental retardation from a survey of 500 individuals with retinoblastoma.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1977377

23 September 2018

Oncogenic point mutations in the human retinoblastoma gene: their application to genetic counseling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1977377

23 September 2018

Prenatal exclusion of hereditary retinoblastoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/1350208

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prediction of familial predisposition to retinoblastoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/1350208

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetics of retinoblastoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/1350208

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/1350208

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion of chromosome region 13q14 is transmissible and does not always predispose to retinoblastoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/1350208

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletions of the esterase D locus from a survey of 200 retinoblastoma patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/1350208

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetics of retinoblastoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/1350208

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1038/BJC.1992.150

1 reference

Europe PubMed Central

11 August 2017

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0 references

1 reference

Europe PubMed Central

11 August 2017

1 reference

Europe PubMed Central

11 August 2017

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0 references

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