(Q34059646)

30 July 2017

Distinct RB1 gene mutations with low penetrance in hereditary retinoblastoma (English)

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30 July 2017

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Lohmann DR

1

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30 July 2017

Brandt B

2

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30 July 2017

Höpping W

3

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30 July 2017

Passarge E

4

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30 July 2017

Horsthemke B

5

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30 July 2017

1 October 1994

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30 July 2017

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30 July 2017

94

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30 July 2017

349-354

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30 July 2017

4

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https://scigraph.springernature.com/pub.10.1007/bf00201591

30 July 2017

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cites work

Mutation and cancer: statistical study of retinoblastoma

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12 December 2020

Molecular mechanisms of oncogenic mutations in tumors from patients with bilateral and unilateral retinoblastoma

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12 December 2020

Mutation theory of carcinogenesis in retinoblastoma

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12 December 2020

Detection of small RB1 gene deletions in retinoblastoma by multiplex PCR and high-resolution gel electrophoresis

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12 December 2020

Hereditary retinoblastoma: delayed mutation or host resistance?

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12 December 2020

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

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12 December 2020

Inherited predisposition to cancer

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12 December 2020

Oncogenic germ-line mutations in Sp1 and ATF sites in the human retinoblastoma gene

1 reference

12 December 2020

Familial, EsD-linked, retinoblastoma with reduced penetrance and variable expressivity.

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12 December 2020

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

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12 December 2020

Mechanisms of loss of heterozygosity in retinoblastoma

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12 December 2020

Molecular etiology of low-penetrance retinoblastoma in two pedigrees.

1 reference

12 December 2020

Characterization of a chicken cDNA encoding the retinoblastoma gene product.

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12 December 2020

Complete or partial homozygosity of chromosome 13 in primary retinoblastoma

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12 December 2020

Characterization of deletions at the retinoblastoma locus in patients with bilateral retinoblastoma

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12 December 2020

Oncogenic point mutations in the human retinoblastoma gene: their application to genetic counseling

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12 December 2020

The mutational spectrum of single base-pair substitutions causing human genetic disease: patterns and predictions

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12 December 2020

Detecting single base substitutions as heteroduplex polymorphisms

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12 December 2020

Epigenetic changes may contribute to the formation and spontaneous regression of retinoblastoma

1 reference

12 December 2020

Structure and expression of the murine retinoblastoma gene and characterization of its encoded protein

1 reference

12 December 2020

Novel non-templated nucleotide addition reactions catalyzed by procaryotic and eucaryotic DNA polymerases

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12 December 2020

Complete genomic sequence of the human retinoblastoma susceptibility gene

1 reference

12 December 2020

Loss of heterozygosity on chromosome 13 and its association with delayed growth of retinoblastoma

1 reference

12 December 2020

Oncogenic point mutations in exon 20 of the RB1 gene in families showing incomplete penetrance and mild expression of the retinoblastoma phenotype

1 reference

12 December 2020

Identification of germline mutations in the RB1 gene by denaturant gradient gel electrophoresis and polymerase chain reaction direct sequencing

1 reference

12 December 2020

Molecular characterization of the retinoblastoma susceptibility gene

1 reference

12 December 2020

Pseudo low penetrance in retinoblastoma. Fortuitous familial aggregation of sporadic cases caused by independently derived mutations in two large pedigrees

1 reference

12 December 2020

Application of linkage analysis to genetic counselling in families with hereditary retinoblastoma

1 reference

12 December 2020

A simple and nonradioactive method for detecting the Rb1.20 DNA polymorphism in the retinoblastoma gene

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00201591

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Dimensions Publication ID

30 July 2017

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