(Q59053447)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2991766%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

title

Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2991766%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

3

Neal G. Copeland

0 references

Nancy A. Jenkins

4

object named as

Nancy A. Jenkins

0 references

author name string

A Koufos

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2991766%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

M F Hansen

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2991766%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

N G Copeland

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2991766%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

N A Jenkins

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2991766%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

B C Lampkin

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2991766%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

W K Cavenee

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2991766%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

language of work or name

English

0 references

publication date

1 July 1985

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2991766%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2991766%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

volume

316

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2991766%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

page(s)

330-334

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2991766%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

issue

6026

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2991766%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/316330a0

8 October 2019

exact match

0 references

cites work

Second primary neoplasms in children

1 reference

Wiedemann-Beckwith syndrome: autosomal-dominant inheritance in a family

21 January 2018

1 reference

7 January 2021

Complete and incomplete forms of Beckwith-Wiedemann syndrome: their oncogenic potential

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7 January 2021

Wilms' tumor and adrenocortical carcinoma with hemihypertrophy and hamartomas

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7 January 2021

ASSOCIATION OF WILMS'S TUMOR WITH ANIRIDIA, HEMIHYPERTROPHY AND OTHER CONGENITAL MALFORMATIONS

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7 January 2021

Fetal rhabdomyomatous nephroblastoma—A variant of Wilms' tumor

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7 January 2021

Total right hepatic lobectomy for rhabdomyosarcoma

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7 January 2021

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

1 reference

7 January 2021

Development of homozygosity for chromosome 11p markers in Wilms' tumour

1 reference

7 January 2021

Loss of a Harvey ras allele in sporadic Wilms' tumour

1 reference

7 January 2021

Somatic deletion and duplication of genes on chromosome 11 in Wilms' tumours.

1 reference

7 January 2021

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

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7 January 2021

Genetic origin of mutations predisposing to retinoblastoma

1 reference

7 January 2021

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

1 reference

7 January 2021

A highly polymorphic locus in human DNA

1 reference

7 January 2021

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

1 reference

7 January 2021

Trisomy 11p15 and Beckwith-Wiedemann syndrome. A report of two cases.

1 reference

7 January 2021

Construction of linkage maps with DNA markers for human chromosomes.

1 reference

7 January 2021

DNA Markers for Nervous System Diseases

1 reference

7 January 2021

Report of the Committee on the Genetic Constitution of Chromosomes 10, 11, and 12.

1 reference

7 January 2021

The highly polymorphic region near the human insulin gene is composed of simple tandemly repeating sequences.

1 reference

7 January 2021

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

1 reference

7 January 2021

Nonrandom association of polymorphic restriction sites in the β-globin gene cluster

1 reference

7 January 2021