Parental origin of mutations of the retinoblastoma gene (Q59093966)

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4 October 2019

title

Parental origin of mutations of the retinoblastoma gene (English)

1 reference

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4 October 2019

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Dryja TP

1

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4 October 2019

Mukai S

2

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4 October 2019

Petersen R

3

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4 October 2019

Rapaport JM

4

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4 October 2019

Walton D

5

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4 October 2019

Yandell DW

6

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4 October 2019

language of work or name

English

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publication date

1 June 1989

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4 October 2019

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4 October 2019

volume

339

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4 October 2019

issue

6225

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4 October 2019

page(s)

556-558

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Mutation and cancer: statistical study of retinoblastoma

4 October 2019

cites work

1 reference

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A general theory of carcinogenesis

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Oncogenes and tumor-suppressing genes

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Molecular detection of deletions involving band q14 of chromosome 13 in retinoblastomas

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

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Human retinoblastoma susceptibility gene: cloning, identification, and sequence

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7 January 2021

Structural evidence for the authenticity of the human retinoblastoma gene

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7 January 2021

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

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7 January 2021

Homozygosity of chromosome 13 in retinoblastoma

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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

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7 January 2021

Genomic imprinting and embryonal tumours

1 reference

7 January 2021

Types, rates, origin and expressivity of chromosome mutations involving 13q14 in retinoblastoma patients.

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7 January 2021

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

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7 January 2021

Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11.

1 reference

7 January 2021

Lack of linkage of familial Wilms' tumour to chromosomal band 11 p13

1 reference

7 January 2021

Prediction of the Risk of Hereditary Retinoblastoma, Using DNA Polymorphisms within the Retinoblastoma Gene

1 reference

7 January 2021

Human retinoblastoma susceptibility gene: genomic organization and analysis of heterozygous intragenic deletion mutants

1 reference

7 January 2021

Chromosome 13 restriction fragment length polymorphisms

1 reference

7 January 2021