(Q39145519)

9 September 2017

1 reference

title

The molecular genetics of retinoblastoma and Wilms' tumor (English)

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9 September 2017

1 reference

Cowell J

1

1 reference

PubMed ID

2822271

9 September 2017

Pritchard J

series ordinal

2

1 reference

9 September 2017

1 January 1987

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Critical Reviews in Oncology Hematology

9 September 2017

1 reference

9 September 2017

7

1 reference

9 September 2017

2

1 reference

9 September 2017

153-168

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Dominant susceptibility to cancer in man.

9 September 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Mutation and cancer: statistical study of retinoblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

The electroencephalogram (EEG) as a research tool in human behavior genetics: psychological examinations in healthy males with various inherited EEG variants. I. Rationale of the study. Material. Methods. Heritability of test parameters

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Deletions of the esterase D locus from a survey of 200 retinoblastoma patients

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Partial triplication and deletion of 13q: study of a family presenting with bilateral retinoblastomas

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Familial Retinoblastoma and Chromosome 13 Deletion Transmitted via an Insertional Translocation

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Cytogenetic forms of retinoblastoma: their incidence in a survey of 66 patients

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Genetic and cytogenetic studies in children with retinoblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Regional assignment of genes for human esterase D and retinoblastoma to chromosome band 13q14

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Retinoblastoma, deletion 13q14, and esterase D: application of gene dosage effect to prenatal diagnosis

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Separation of retinoblastoma and esterase D loci in a patient with sporadic retinoblastoma and del(13)(q14.1q22.3)

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Retinoblastoma-del(13q14): Report of two patients, one with a trisomic sib due to maternal insertion. Gene-dosage effect for esterase D

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

High rate of detection of 13q14 deletion mosaicism among retinoblastoma patients (using more extensive methods)

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Regional mapping of catalase and Wilms tumor--aniridia, genitourinary abnormalities, and mental retardation triad loci to the chromosome segment 11p1305----p1306.

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Wilms's tumour and aniridia: clinical and cytogenetic features

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Aniridia, cataract and gonadoblastoma in a mentally retarded girl with deletion of chromosome II. A clinicopathological case report

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Aniridia, male pseudohermaphroditism, gonadoblastoma, mental retardation, and del 11p13.

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Del11p13/nephroblastoma without aniridia

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Computer-assisted analysis of chromosomal abnormalities: detection of a deletion in aniridia-Wilms' tumor syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Familial occurrence of the aniridia-Wilms tumor syndrome with deletion 11p13-14.1

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Multiple karyotypic changes in retinoblastoma tumor cells: Presence of normal chromosome No. 13 in most tumors

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Cytogenetic analysis of retinoblastoma: evidence for multifocal origin and in vivo gene amplification

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Retinoblastoma A Model of Hereditary Fragile Chromosomal Regions

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

A deleted chromosome no. 13 in human retinoblastoma cells: relevance to tumorigenesis

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Nonrandom chromosomal changes in untreated retinoblastomas

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Isochromosome 6p, a unique chromosomal abnormality in retinoblastoma: Verification by standard staining techniques, new densitometric methods, and somatic cell hybridization

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Further chromosome studies on Wilms' tumor cells of patients without aniridia

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Chromosome number 11 and Wilms' tumor

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Abnormalities of chromosomes 1 and 11 in Wilms' tumor

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

A cytogenetic study of Wilms' tumor

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Somatic cell hybrid mapping panels

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

DNA content and DNA-based centromeric index of the 24 human chromosomes

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Construction and characterization of genomic libraries from specific human chromosomes

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Cloning of a representative genomic library of the human X chromosome after sorting by flow cytometry

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Homozygosity of chromosome 13 in retinoblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Isolation of human chromosome 13-specific DNA sequences cloned from flow sorted chromosomes and potentially linked to the retinoblastoma locus

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Genetic origin of mutations predisposing to retinoblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

A mitotic recombination in Wilms tumor occurs between the parathyroid hormone locus and 11p13

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Prediction of familial predisposition to retinoblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Isolation of amplified DNA sequences from IMR-32 human neuroblastoma cells: facilitation by fluorescence-activated flow sorting of metaphase chromosomes

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Transposition and amplification of oncogene-related sequences in human neuroblastomas

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

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/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Double minutes and homogeneously staining regions: gene amplification in mammalian cells

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Molecular and cytologic analysis of DNA amplification in retinoblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

A detailed analysis of chromosomal changes in heritable and non-heritable retinoblastoma.

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Expression and amplification of the N-myc gene in primary retinoblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Onco gen: Human oncogene locations and chromosome aberrations

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

The c-Ha-ras1, insulin and β-globin loci map outside the deletion associated with aniridia-Wilms' tumour

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Insulin-like growth factor-II gene expression in Wilms' tumour and embryonic tissues.

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Pleiotropic effects of the gene for retinoblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Familial osteosarcoma associated with 13;14 chromosomal rearrangement

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

Osteosarcoma and retinoblastoma: a shared chromosomal mechanism revealing recessive predisposition

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2887%2980024-0

7 January 2021

10.1016/S1040-8428(87)80024-0

Identifiers

DOI

1 reference

9 September 2017

1 reference

PubMed ID

2822271