(Q72228209)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8102298%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

title

Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplification (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8102298%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

1 reference

10

1 reference

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25 October 2019

author name string

Caron H

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8102298%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

van Sluis P

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8102298%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

van Hoeve M

3

1 reference

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25 October 2019

de Kraker J

4

1 reference

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25 October 2019

Bras J

5

1 reference

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25 October 2019

Slater R

6

1 reference

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25 October 2019

Mannens M

7

1 reference

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25 October 2019

Voûte PA

8

1 reference

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25 October 2019

Westerveld A

9

1 reference

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25 October 2019

publication date

1 June 1993

1 reference

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25 October 2019

1 reference

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25 October 2019

volume

4

1 reference

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25 October 2019

issue

2

1 reference

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25 October 2019

page(s)

187-190

1 reference

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https://scigraph.springernature.com/pub.10.1038/ng0693-187

25 October 2019

exact match

0 references

cites work

Neuroblastoma. Effect of genetic factors on prognosis and treatment

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-187

7 January 2021

Neuroblastoma consensus deletion maps to 1p36.1-2.

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-187

7 January 2021

Loss of alleles from the distal short arm of chromosome 1 occurs late in melanoma tumor progression

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-187

7 January 2021

Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-187

7 January 2021

A model for embryonal rhabdomyosarcoma tumorigenesis that involves genome imprinting

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-187

7 January 2021

Preferential mutation of paternally derived RB gene as the initial event in sporadic osteosarcoma.

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-187

7 January 2021

Genomic imprinting and genetic disorders in man.

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-187

7 January 2021

Parental origin of mutations of the retinoblastoma gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-187

7 January 2021

Preferential mutation of the neurofibromatosis type 1 gene in paternally derived chromosomes

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-187

7 January 2021

Preferential germline mutation of the paternal allele in retinoblastoma

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-187

7 January 2021

Familial neuroblastoma. Case reports, literature review, and etiologic considerations

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-187

7 January 2021

Familial occurrence of neuroblastoma, von Recklinghausen's neurofibromatosis, Hirschsprung's agangliosis and jaw-winking syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-187

7 January 2021

Familial neural crest tumours

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-187

7 January 2021

Transgenes as molecular probes for genomic imprinting.

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-187

7 January 2021

Imprinting and Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-187

7 January 2021

N-myc expression switched off and class I human leukocyte antigen expression switched on after somatic cell fusion of neuroblastoma cells

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-187

7 January 2021

A proposed staging for children with neuroblastoma.Children's cancer study group A

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-187

7 January 2021

Amplified DNA with limited homology to myc cellular oncogene is shared by human neuroblastoma cell lines and a neuroblastoma tumour

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-187

7 January 2021

The CEPH consortium linkage map of human chromosome 1

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-187

7 January 2021

Identifiers

DOI

10.1038/NG0693-187

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8102298%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

1 reference