(Q35198154)

7 August 2017

title

Parental origin of de novo constitutional deletions of chromosomal band 11p13 (English)

1 reference

7 August 2017

V Huff

1

1 reference

7 August 2017

A Meadows

2

1 reference

7 August 2017

V M Riccardi

3

1 reference

7 August 2017

L C Strong

4

1 reference

7 August 2017

G F Saunders

5

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 July 1990

1 reference

American Journal of Human Genetics

7 August 2017

published in

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7 August 2017

volume

47

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7 August 2017

issue

1

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7 August 2017

page(s)

155-160

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A systematic approach for detecting high-frequency restriction fragment length polymorphisms using large genomic probes

7 August 2017

cites work

1 reference

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The association between parental occupation and childhood malignancy

28 July 2018

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Childhood cancer and occupational radiation exposure in parents

28 July 2018

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Mutation and cancer: a model for Wilms' tumor of the kidney

28 July 2018

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Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome

28 July 2018

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A case report of a patient with retinoblastoma and chromosome 13q deletion: assignment of a new gene (gene for LCP1) on human chromosome 13.

28 July 2018

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Isolation and characterization of the human catalase gene

28 July 2018

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

28 July 2018

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Molecular cytogenetics: toward dissection of the contiguous gene syndromes

28 July 2018

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Genetic mechanisms of tumor-specific loss of 11p DNA sequences in Wilms tumor

28 July 2018

1 reference

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An RFLP associated with the human catalase gene

28 July 2018

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An EcoRI polymorphism associated with a human genomic clone from band 11p13.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683741

Nonrandom loss of maternal chromosome 11 alleles in Wilms tumors

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683741

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

28 July 2018

1 reference

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Long range physical map of the Wilms' tumor-aniridia region on human chromosome 11.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683741

Age distribution of Wilms' tumor: report from the National Wilms' Tumor Study.

28 July 2018

1 reference

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Molecular definition of de novo and genetically transmitted WAGR-associated rearrangements of 11p13.

28 July 2018

1 reference

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Paternal origin of new mutations in von Recklinghausen neurofibromatosis.

28 July 2018

1 reference

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A BglII RFLP detected by the probe JA8-1 at human chromosome band 11p13 (D11S417)

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683741

A panel of restriction fragment length polymorphisms for chromosomal band 11p13.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683741

Occupations of fathers of patients with Wilms's tumour

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683741

Aniridia Caused by a Heritable Chromosome 11 Deletion

28 July 2018

1 reference

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683741

Chromosomal imbalance in the Aniridia-Wilms' tumor association: 11p interstitial deletion

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683741

Duplication 11p11.3 leads to 14.1 to meiotic crossing--over.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683741

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

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683741

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

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683741

A highly polymorphic locus cloned from the breakpoint of a chromosome 11p13 deletion associated with the WAGR syndrome

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683741

Preferential germline mutation of the paternal allele in retinoblastoma

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683741

Parental origin of de novo chromosome rearrangements

15 November 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/1971994

12 December 2020

Genetics of Wilms' tumor

1 reference

https://pubmed.ncbi.nlm.nih.gov/1971994

12 December 2020

Interstitial deletion of short arm of chromosome 11 limited to Wilms' tumor cells in a patient without aniridia

1 reference

https://pubmed.ncbi.nlm.nih.gov/1971994

12 December 2020

Wilms tumor with aniridia/iris dysplasia and apparently normal chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/1971994

12 December 2020

Epidemiological features of Wilms' tumor: results of the National Wilms' Tumor Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/1971994

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1971994

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1971994

12 December 2020

Loss of a Harvey ras allele in sporadic Wilms' tumour

1 reference

https://pubmed.ncbi.nlm.nih.gov/1971994

12 December 2020

Clinical and cytogenetic studies of the Prader-Willi syndrome: evidence of phenotype-karyotype correlation

1 reference

https://pubmed.ncbi.nlm.nih.gov/1971994

12 December 2020

High-resolution studies in patients with aniridia-Wilms tumor association

1 reference

https://pubmed.ncbi.nlm.nih.gov/1971994

12 December 2020

The anonymous RFLP locus D11S16 is tightly linked to catalase on 11p

1 reference

https://pubmed.ncbi.nlm.nih.gov/1971994

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1971994

12 December 2020

Aniridia—Wilms tumor association

1 reference

https://pubmed.ncbi.nlm.nih.gov/1971994

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1971994

12 December 2020

Parental occupation and Wilms' tumor: results of a case-control study

1 reference

https://pubmed.ncbi.nlm.nih.gov/1971994

12 December 2020

Maternal allele loss in Wilms' tumour

1 reference

https://pubmed.ncbi.nlm.nih.gov/1971994

12 December 2020

Parental origin of mutations of the retinoblastoma gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/1971994

12 December 2020

Spontaneous mutation in man

1 reference

https://pubmed.ncbi.nlm.nih.gov/1971994

12 December 2020

Identifiers

PMC publication ID

1683741

1 reference

7 August 2017

1 reference