Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5. (Q35248366)

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30 September 2019

title

Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5. (English)

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30 September 2019

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Koufos A

1

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30 September 2019

Grundy P

2

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30 September 2019

Morgan K

3

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30 September 2019

Aleck KA

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30 September 2019

Hadro T

5

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30 September 2019

Lampkin BC

6

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30 September 2019

Kalbakji A

7

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30 September 2019

Cavenee WK

8

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30 September 2019

language of work or name

English

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publication date

1 May 1989

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American Journal of Human Genetics

30 September 2019

published in

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30 September 2019

volume

44

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30 September 2019

page(s)

711-719

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30 September 2019

issue

5

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ASSOCIATION OF WILMS'S TUMOR WITH ANIRIDIA, HEMIHYPERTROPHY AND OTHER CONGENITAL MALFORMATIONS

30 September 2019

cites work

1 reference

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

27 July 2018

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Isolation and preliminary characterization of a human transforming gene from T24 bladder carcinoma cells

27 July 2018

1 reference

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

27 July 2018

1 reference

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Nonrandom association of polymorphic restriction sites in the β-globin gene cluster

27 July 2018

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Polymorphic DNA region adjacent to the 5' end of the human insulin gene

27 July 2018

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A locus on chromosome 11p with multiple restriction site polymorphisms

27 July 2018

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Exomphalos-Macroglossia-Gigantism Syndrome in Jamaican Infants

27 July 2018

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The Wiedemann-Beckwith syndrome: genetic considerations and a diagnostic sign.

27 July 2018

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Wiedemann-Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literature

27 July 2018

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

27 July 2018

1 reference

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

27 July 2018

1 reference

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An RFLP associated with the human catalase gene

27 July 2018

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Genomic imprinting and carcinogenesis

27 July 2018

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

27 July 2018

1 reference

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

27 July 2018

1 reference

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Loss of alleles on the short arm of chromosome 11 in a hepatoblastoma from a child with Beckwith-Wiedemann syndrome.

27 July 2018

1 reference

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Studies of malformation syndromes of man XXIX: the Wiedemann-Beckwith syndrome. Clinical, genetic and pathogenetic studies of 12 cases

27 July 2018

1 reference

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

27 July 2018

1 reference

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Neoplasms associated with the Beckwith-Wiedemann syndrome

27 July 2018

1 reference

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FAMILIAL MALFORMATION COMPLEX WITH UMBILICAL HERNIA AND MACROGLOSSIA--A "NEW SYNDROME"?

27 July 2018

1 reference

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

26 September 2018

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Strategies for multilocus linkage analysis in humans

26 September 2018

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

26 September 2018

1 reference

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

26 September 2018

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Restriction sites containing CpG show a higher frequency of polymorphism in human DNA

26 September 2018

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Loss of a Harvey ras allele in sporadic Wilms' tumour

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12 December 2020

Localization of the polymorphic human calcitonin gene on chromosome 11

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12 December 2020

Restriction fragment length polymorphisms at the human parathyroid hormone gene locus

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Constitutional interstitial deletion of 11p11 and pericentric inversion of chromosome 9 in a patient with Wiedemann-Beckwith syndrome and hepatoblastoma

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12 December 2020

Deletion of chromosome 11(p11p13) in a patient with Beckwith-Wiedemann syndrome

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12 December 2020

Degree of methylation of transgenes is dependent on gamete of origin

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12 December 2020

Chromosomal localization of the human rhabdomyosarcoma locus by mitotic recombination mapping

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12 December 2020

Generation of homozygosity at the c-Ha-ras-1 locus on chromosome 11p in an adrenal adenoma from an adult with Wiedemann—Beckwith syndrome

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Wiedemann-Beckwith syndrome: autosomal-dominant inheritance in a family

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12 December 2020

Identifiers

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30 September 2019

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