(Q34535432)

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Uniparental paternal disomy in a genetic cancer-predisposing syndrome

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2 August 2017

Uniparental paternal disomy in a genetic cancer-predisposing syndrome (English)

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2 August 2017

author name string

Henry I

1

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2 August 2017

Bonaiti-Pellié C

2

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2 August 2017

Chehensse V

3

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2 August 2017

Beldjord C

4

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2 August 2017

Schwartz C

5

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2 August 2017

Utermann G

6

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2 August 2017

Junien C

7

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2 August 2017

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publication date

1 June 1991

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2 August 2017

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2 August 2017

351

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2 August 2017

6328

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2 August 2017

665-667

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2 August 2017

Molecular definition of the 11p15.5 region involved in Beckwith-Wiedemann syndrome and probably in predisposition to adrenocortical carcinoma

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https://api.crossref.org/works/10.1038%2F351665A0

7 January 2021

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Letter: Autosomal-dominant sex-dependent transmission of the Wiedemann-Beckwith syndrome

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https://api.crossref.org/works/10.1038%2F351665A0

7 January 2021

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

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https://api.crossref.org/works/10.1038%2F351665A0

7 January 2021

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A model for embryonal rhabdomyosarcoma tumorigenesis that involves genome imprinting

1 reference

https://api.crossref.org/works/10.1038%2F351665A0

7 January 2021

based on heuristic

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The Wiedemann-Beckwith syndrome: pedigree studies on five families with evidence for autosomal dominant inheritance with variable expressivity

1 reference

https://api.crossref.org/works/10.1038%2F351665A0

7 January 2021

based on heuristic

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Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.

1 reference

https://api.crossref.org/works/10.1038%2F351665A0

7 January 2021

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The structural gene for aldolase B (ALDB) maps to 9q13----32

1 reference

https://api.crossref.org/works/10.1038%2F351665A0

7 January 2021

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Report of the committee on the genetic constitution of chromosome 11.

1 reference

https://api.crossref.org/works/10.1038%2F351665A0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2F351665A0

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2F351665A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Loss of a Harvey ras allele in sporadic Wilms' tumour

1 reference

https://api.crossref.org/works/10.1038%2F351665A0

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2F351665A0

7 January 2021

based on heuristic

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Chromosomal localization of the human rhabdomyosarcoma locus by mitotic recombination mapping

1 reference

https://api.crossref.org/works/10.1038%2F351665A0

7 January 2021

based on heuristic

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Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma

1 reference

https://api.crossref.org/works/10.1038%2F351665A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic changes in human adrenocortical carcinomas

1 reference

https://api.crossref.org/works/10.1038%2F351665A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/351665A0

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

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