(Q74360482)

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10 November 2019

title

Molecular genetic analysis of familial neuroblastoma (English)

1 reference

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10 November 2019

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9

G M Brodeur

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10 November 2019

1

J M Maris

1 reference

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10 November 2019

author name string

S M Kyemba

2

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10 November 2019

T R Rebbeck

3

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10 November 2019

P S White

4

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10 November 2019

E P Sulman

5

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10 November 2019

S J Jensen

6

1 reference

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10 November 2019

C Allen

7

1 reference

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10 November 2019

J A Biegel

8

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10 November 2019

publication date

1 October 1997

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European Journal of Cancer

10 November 2019

published in

1 reference

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10 November 2019

volume

33

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10 November 2019

issue

12

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10 November 2019

page(s)

1923-1928

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

10 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900265-7

7 January 2021

Mutation and cancer: statistical study of retinoblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900265-7

7 January 2021

A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900265-7

7 January 2021

Constitutional translocation t(1;17)(p36;q12-21) in a patient with neuroblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900265-7

7 January 2021

Deletion of chromosome 11 and of 14q sequences in neuroblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900265-7

7 January 2021

1;17 translocations and other chromosome 17 rearrangements in human primary neuroblastoma tumors and cell lines

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900265-7

7 January 2021

Allelic loss of chromosome 1p as a predictor of unfavorable outcome in patients with neuroblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900265-7

7 January 2021

Ondine-Hirschsprung syndrome (Haddad syndrome). Further delineation in two cases and review of the literature.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900265-7

7 January 2021

Multifocal ganglioneuroblastoma coexistent with total colonic aganglionosis

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900265-7

7 January 2021

Hirschsprung's disease, Ondine's curse, and neuroblastoma--manifestations of neurocristopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900265-7

7 January 2021

The complete spectrum of neurocristopathy in an infant with congenital hypoventilation, Hirschsprung's disease, and neuroblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900265-7

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/10.1016%2FS0959-8049%2897%2900265-7

7 January 2021

Familial neuroblastoma: a three-generation pedigree and a further association with Hirschsprung disease

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900265-7

7 January 2021

Mutations of the RET proto-oncogene in Hirschsprung's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900265-7

7 January 2021

A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900265-7

7 January 2021

Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome)

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900265-7

7 January 2021

A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome)

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900265-7

7 January 2021

Neurofibromatosis and associated neuroectodermal tumors: a congenital neurocristopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900265-7

7 January 2021

Synchronous neuroblastoma and von Recklinghausen's disease: a review of the literature

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900265-7

7 January 2021

Loss of the normal NF1 allele from the bone marrow of children with type 1 neurofibromatosis and malignant myeloid disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900265-7

7 January 2021

Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesis

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900265-7

7 January 2021

Neurofibromatosis type 1 gene mutations in neuroblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900265-7

7 January 2021

A comprehensive genetic map of the human genome based on 5,264 microsatellites

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900265-7

7 January 2021

Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900265-7

7 January 2021

10.1016/S0959-8049(97)00265-7

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9516825%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

1 reference