Osteosarcoma and retinoblastoma: a shared chromosomal mechanism revealing recessive predisposition (Q37542430)

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scientific article published on September 1985

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English	Osteosarcoma and retinoblastoma: a shared chromosomal mechanism revealing recessive predisposition	scientific article published on September 1985

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PMC publication ID

391023

retrieved

20 August 2017

title

Osteosarcoma and retinoblastoma: a shared chromosomal mechanism revealing recessive predisposition (English)

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Europe PubMed Central

PMC publication ID

391023

retrieved

20 August 2017

main subject

retinoblastoma

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based on heuristic

inferred from title

author name string

M F Hansen

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1

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Europe PubMed Central

PMC publication ID

391023

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20 August 2017

A Koufos

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2

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Europe PubMed Central

PMC publication ID

391023

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20 August 2017

B L Gallie

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3

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Europe PubMed Central

PMC publication ID

391023

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20 August 2017

R A Phillips

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4

1 reference

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Europe PubMed Central

PMC publication ID

391023

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20 August 2017

O Fodstad

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5

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Europe PubMed Central

PMC publication ID

391023

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20 August 2017

A Brøgger

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6

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Europe PubMed Central

PMC publication ID

391023

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20 August 2017

T Gedde-Dahl

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7

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Europe PubMed Central

PMC publication ID

391023

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20 August 2017

W K Cavenee

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8

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Europe PubMed Central

PMC publication ID

391023

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20 August 2017

language of work or name

English

0 references

publication date

1 September 1985

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stated in

Europe PubMed Central

PMC publication ID

391023

retrieved

20 August 2017

published in

Proceedings of the National Academy of Sciences of the United States of America

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Europe PubMed Central

PMC publication ID

391023

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20 August 2017

volume

82

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Europe PubMed Central

PMC publication ID

391023

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20 August 2017

issue

18

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Europe PubMed Central

PMC publication ID

391023

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20 August 2017

page(s)

6216-6220

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Europe PubMed Central

PMC publication ID

391023

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20 August 2017

cites work

Isolation and preliminary characterization of a human transforming gene from T24 bladder carcinoma cells

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Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

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PubMed Central

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23 August 2017

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

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Mutation and cancer: statistical study of retinoblastoma

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23 August 2017

Pleiotropic effects of the gene for retinoblastoma

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Loss of polymorphic restriction fragments in malignant melanoma: implications for tumor heterogeneity

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Nonocular cancer in retinoblastoma survivors

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Mutation and childhood cancer: a probabilistic model for the incidence of retinoblastoma

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Second nonocular tumors in retinoblastoma survivors. Are they radiation-induced?

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Report of the Committee on Human Gene Mapping by Recombinant DNA Techniques

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A locus on chromosome 11p with multiple restriction site polymorphisms

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Heredity and cancer in man.

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14 September 2017

Retinoblastoma and Osteogenic Sarcoma

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Multiple primary cancers: review of clinical studies from two Missouri hospitals

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28 September 2017

Retinoblastoma associated with other primary malignant tumours

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Retinoblastoma and osteogenic sarcoma in siblings.

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25 June 2018

Family studies in retinoblastoma

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PubMed Central

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Genetic origin of mutations predisposing to retinoblastoma

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PubMed Central

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25 June 2018

Statistical methods for studying multiple primary malignant neoplasms

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Multiple malignant neoplasms in the Charity Hospital of Louisiana Tumor Registry

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PubMed Central

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Multiple primary cancers at Memorial Hospital 1949-1962.

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25 June 2018

Retinoblastoma and Subband Deletion of Chromosome 13

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PubMed Central

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25 June 2018

Patient with 13 Chromosome Deletion: Evidence That the Retinoblastoma Gene Is a Recessive Cancer Gene

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PubMed Central

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1 September 2018

The heredity of retinoblastoma

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2994066

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Retinoblastoma: epidemiologic characteristics

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2994066

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bilateral Retinoblastoma: A Dominantly Inherited Affection

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2994066

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal deletion and retinoblastoma

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2994066

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Late extraocular tumours in retinoblastoma survivors

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2994066

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormalities of chromosome #13 in retinoblastomas from individuals with normal constitutional karyotypes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2994066

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene for hereditary retinoblastoma assigned to human chromosome 13 by linkage to esterase D

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2994066

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Somatic inactivation of genes on chromosome 13 is a common event in retinoblastoma

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2994066

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Restriction sites containing CpG show a higher frequency of polymorphism in human DNA

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2994066

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome 13 restriction fragment length polymorphisms

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2994066

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygosity of chromosome 13 in retinoblastoma

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2994066

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of alleles at loci on human chromosome 11 during genesis of Wilms' tumour

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2994066

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1073/PNAS.82.18.6216

1 reference

stated in

Europe PubMed Central

PMC publication ID

391023

retrieved

20 August 2017

ADS bibcode

1985PNAS...82.6216H

0 references

PMC publication ID

391023

1 reference

stated in

Europe PubMed Central

PMC publication ID

391023

retrieved

20 August 2017

PubMed publication ID

2994066

1 reference

stated in

Europe PubMed Central

PMC publication ID

391023

retrieved

20 August 2017

ResearchGate publication ID

20162344

0 references

 

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