(Q52068403)

21 April 2018

title

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

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21 April 2018

author name string

Grundy P

1

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21 April 2018

Koufos A

2

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21 April 2018

Morgan K

3

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21 April 2018

Li FP

4

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21 April 2018

Meadows AT

5

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21 April 2018

Cavenee WK

6

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21 April 2018

language of work or name

English

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publication date

1 November 1988

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21 April 2018

published in

Nature

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21 April 2018

volume

336

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21 April 2018

page(s)

374-376

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21 April 2018

issue

6197

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21 April 2018

https://scigraph.springernature.com/pub.10.1038/336374a0

exact match

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cites work

Genetics of Wilms' tumor

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Loss of a Harvey ras allele in sporadic Wilms' tumour

1 reference

7 January 2021

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

1 reference

7 January 2021

Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome

1 reference

7 January 2021

Trisomy 11p15 and Beckwith-Wiedemann syndrome. A report of two cases.

1 reference

7 January 2021

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

1 reference

7 January 2021

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

1 reference

7 January 2021

Report of the Committee on the Genetic Constitution of Chromosomes 10, 11, and 12

1 reference

7 January 2021

Molecular analysis of chromosome 11 deletions in aniridia-Wilms tumor syndrome

1 reference

7 January 2021

Report of the committee on the genetic constitution of chromosomes 10, 11, and 12

1 reference

7 January 2021

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

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7 January 2021

Strategies for multilocus linkage analysis in humans

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7 January 2021

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

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7 January 2021

Wilms's tumor in three children of a woman with congenital hemihypertrophy.

1 reference

7 January 2021

Deletion of genes on chromosome 1 in endocrine neoplasia

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7 January 2021

Genomic imprinting and carcinogenesis

1 reference

7 January 2021

Introduction of a normal human chromosome 11 into a Wilms' tumor cell line controls its tumorigenic expression

1 reference

7 January 2021

The beta-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus.

1 reference

7 January 2021

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

1 reference

7 January 2021

An RFLP associated with the human catalase gene

1 reference

7 January 2021

DNA sequence and regional assignment of the human follicle-stimulating hormone beta-subunit gene to the short arm of human chromosome 11

1 reference

7 January 2021

Localization of the polymorphic human calcitonin gene on chromosome 11

1 reference

7 January 2021

Restriction fragment length polymorphisms at the human parathyroid hormone gene locus

1 reference

7 January 2021

DNA sequence variants in the G gamma-, A gamma-, delta- and beta-globin genes of man

1 reference

7 January 2021

A simple scheme for the analysis of HLA linkages in pedigrees

1 reference

7 January 2021

Identifiers

DOI

10.1038/336374A0

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21 April 2018

Dimensions Publication ID

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21 April 2018