(Q33195114)

23 July 2017

1 reference

title

Abnormal constitutional karyotypes in patients with neuroblastoma: a report of four new cases and review of 47 others in the literature (English)

1 reference

23 July 2017

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1 reference

Kathy Pritchard-Jones

5

object named as

Kathy Pritchard-Jones

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23 July 2017

3

Charles A Stiller

1 reference

23 July 2017

Daniel Satgé

1

1 reference

23 July 2017

Sam W Moore

2

1 reference

23 July 2017

Félix K Niggli

4

1 reference

23 July 2017

Nick Bown

6

1 reference

23 July 2017

Jean Bénard

7

1 reference

23 July 2017

Dominique Plantaz

8

1 reference

23 July 2017

publication date

1 December 2003

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Cancer Genetics and Cytogenetics

23 July 2017

published in

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23 July 2017

volume

147

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23 July 2017

issue

2

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23 July 2017

page(s)

89-98

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Aniridia-Wilms’ tumor association: evidence for specific deletion of 11p13

23 July 2017

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7 January 2021

A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma

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7 January 2021

Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping

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7 January 2021

Molecular biology and genetics of human neuroblastoma

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7 January 2021

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

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7 January 2021

Chromosomal aberrations in human neuroblastomas

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7 January 2021

Abnormalities of chromosome 1p in human neuroblastoma tumors and cell lines

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7 January 2021

Homozygous deletion of the neurofibromatosis-1 gene in the tumor of a patient with neuroblastoma

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7 January 2021

Identical chromosome 1p breakpoint abnormality in both the tumor and the constitutional karyotype of a patient with neuroblastoma

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7 January 2021

Neuroblastoma and related tumors in Turner's syndrome

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7 January 2021

Causes of death in X chromatin positive males (Klinefelter's syndrome).

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7 January 2021

Cancer incidence in men with Klinefelter syndrome.

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7 January 2021

Abnormal number of X chromosomes and neuroblastic tumors

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7 January 2021

A case of Down's syndrome associated with progressive extradural neuroblastoma

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7 January 2021

Risks of leukaemia and solid tumours in individuals with Down's syndrome.

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7 January 2021

Pattern of malignant disorders in individuals with Down's syndrome.

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7 January 2021

Neurite extension and neuronal survival activities of recombinant S100 beta proteins that differ in the content and position of cysteine residues

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7 January 2021

A decreased incidence of neuroblastomas in Down's syndrome and overproduction of S-100 b protein

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7 January 2021

High serum endostatin levels in Down syndrome: implications for improved treatment and prevention of solid tumours

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7 January 2021

High incidence of constitutional balanced translocations in neuroblastoma

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7 January 2021

Trisomy 2p: analysis of unusual phenotypic findings

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7 January 2021

Neuroblastoma in a dysmorphic girl with a partial duplication of 2p caused by an unbalanced translocation

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7 January 2021

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

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7 January 2021

Amplification of N-myc in untreated human neuroblastomas correlates with advanced disease stage

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7 January 2021

Neuroblastoma tumour genetics: clinical and biological aspects

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https://api.crossref.org/works/10.1016%2FS0165-4608%2803%2900203-6

7 January 2021

Targeted expression of MYCN causes neuroblastoma in transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2803%2900203-6

7 January 2021

Patterns of oncogene activation in human neuroblastoma cells

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2803%2900203-6

7 January 2021

Chromosome 2 short arm translocations revealed by M-FISH analysis of neuroblastoma cell lines

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7 January 2021

Multicentre analysis of patterns of DNA gains and losses in 204 neuroblastoma tumors: how many genetic subgroups are there?

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7 January 2021

Allelic loss of chromosome 1 and additional chromosome 17 material are both unfavourable prognostic markers in neuroblastoma

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7 January 2021

Gain of chromosome arm 17q and adverse outcome in patients with neuroblastoma

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7 January 2021

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

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7 January 2021

Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndrome

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7 January 2021

The N-myc and c-myc downstream pathways include the chromosome 17q genes nm23-H1 and nm23-H2.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2803%2900203-6

7 January 2021

Characterisation of the chromosome breakpoints in a patient with a constitutional translocation t(1;17)(p36.31-p36.13;q11.2-q12) and neuroblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2803%2900203-6

7 January 2021

Allelic deletion at 11q23 is common in MYCN single copy neuroblastomas

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2803%2900203-6

7 January 2021

Comparative genomic hybridization (CGH) analysis of stage 4 neuroblastoma reveals high frequency of 11q deletion in tumors lackingMYCN amplification

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2803%2900203-6

7 January 2021

Neuroblastoma in a boy with MCA/MR syndrome, deletion 11q, and duplication 12q.

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7 January 2021

Familial neuroblastoma

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7 January 2021

Localization of a hereditary neuroblastoma predisposition gene to 16p12-p13

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7 January 2021

Analysis of loss of heterozygosity at 16p12-p13 (familial neuroblastoma locus) in 470 neuroblastomas including both sporadic and mass screening tumors

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7 January 2021

A case of partial 2p trisomy with neuroblastoma

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7 January 2021

Autosomal dominant congenital cataract and microphthalmia associated with a familial t(2;16) translocation

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7 January 2021

The p16 (CDKN2A) gene is involved in the growth of neuroblastoma cells and its expression is associated with prognosis of neuroblastoma patients

1 reference

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7 January 2021

Microscopic neuroblastoma in a fetus with a de novo unbalanced translocation 3;10

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7 January 2021

Normal variation at the myotonic dystrophy locus in global human populations

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7 January 2021

Inherited partial trisomy #15 complicated by neuroblastoma

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7 January 2021

Chromosomal locations and modes of action of genes of the retinoid (vitamin A) system support their involvement in the etiology of schizophrenia

1 reference

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7 January 2021

Functional roles of S100 proteins, calcium-binding proteins of the EF-hand type

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7 January 2021

The DNA sequence of human chromosome 21

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7 January 2021

Childhood cancer and congenital defects. A study of U.S. death certificates during the period 1960-1966.

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7 January 2021

A case of mosaic Down's syndrome concomitant with ganglioneuroma

1 reference

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7 January 2021

Excess of congenital abnormalities in French-Canadian children with neuroblastoma: a case series study from Montréal.

1 reference

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7 January 2021

Brief report: Neuroblastoma in Down syndrome

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7 January 2021

Acute plasmacytic interstitial nephritis in a child with Down syndrome

1 reference

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7 January 2021

Two cases of trisomy D associated with adrenal tumours

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7 January 2021

Nongonadal neoplasia in Turner's syndrome

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7 January 2021

Neuroblastoma with opsomyoclonus and Turner syndrome

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7 January 2021

Anti-Hu antibody in a neuroblastoma-associated paraneoplastic syndrome.

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7 January 2021

Ganglioneuroma of left adrenal gland in a patient with Turner syndrome during growth hormone therapy

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2803%2900203-6

7 January 2021

Simultaneous adrenocortical carcinoma and ganglioneuroblastoma in a child with Turner syndrome and germline p53 mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2803%2900203-6

7 January 2021

Turner syndrome and ganglioneuroma

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2803%2900203-6

7 January 2021

Trisomy 18 and neurogenic neoplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2803%2900203-6

7 January 2021

Molecular characterization of a (1;10)(p22;q21) constitutional translocation from a patient with neuroblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2803%2900203-6

7 January 2021

Molecular characterization of the 1p22 breakpoint region spanning the constitutional translocation breakpoint in a neuroblastoma patient with a t(1;10)(p22;q21)

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2803%2900203-6

7 January 2021

NB4S, a member of the TBC1 domain family of genes, is truncated as a result of a constitutional t(1;10)(p22;q21) chromosome translocation in a patient with stage 4S neuroblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2803%2900203-6

7 January 2021

Cytogenetic investigations of solid tumours of children

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2803%2900203-6

7 January 2021

Molecular analysis of the region of distal 1p commonly deleted in neuroblastoma.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2803%2900203-6

7 January 2021

Neuroblastoma in monozygotic twins--a case of probable twin-to-twin metastasis

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2803%2900203-6

7 January 2021

Germline duplication of chromosome 2p and neuroblastoma.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2803%2900203-6

7 January 2021

Dup 3(q) syndrome and neuroblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2803%2900203-6

7 January 2021

Genetics of familial neuroblastoma: long-range studies

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2803%2900203-6

7 January 2021

46,XY/47,XY, + 17p + mosaicism in amniocytes associated with fetal abnormalities despite normal fetal blood karyotype

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2803%2900203-6

7 January 2021

10.1016/S0165-4608(03)00203-6

Identifiers

DOI

1 reference

23 July 2017

1 reference