(Q35248366)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2539717%20AND%20SRC:MED&resulttype=core&format=json

30 September 2019

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2539717%20AND%20SRC:MED&resulttype=core&format=json

30 September 2019

1 reference

Koufos A

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2539717%20AND%20SRC:MED&resulttype=core&format=json

30 September 2019

Grundy P

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2539717%20AND%20SRC:MED&resulttype=core&format=json

30 September 2019

Morgan K

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2539717%20AND%20SRC:MED&resulttype=core&format=json

30 September 2019

Aleck KA

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2539717%20AND%20SRC:MED&resulttype=core&format=json

30 September 2019

Hadro T

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2539717%20AND%20SRC:MED&resulttype=core&format=json

30 September 2019

Lampkin BC

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2539717%20AND%20SRC:MED&resulttype=core&format=json

30 September 2019

Kalbakji A

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2539717%20AND%20SRC:MED&resulttype=core&format=json

30 September 2019

Cavenee WK

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2539717%20AND%20SRC:MED&resulttype=core&format=json

30 September 2019

language of work or name

English

0 references

publication date

1 May 1989

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2539717%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Human Genetics

30 September 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2539717%20AND%20SRC:MED&resulttype=core&format=json

30 September 2019

volume

44

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2539717%20AND%20SRC:MED&resulttype=core&format=json

30 September 2019

page(s)

711-719

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2539717%20AND%20SRC:MED&resulttype=core&format=json

30 September 2019

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2539717%20AND%20SRC:MED&resulttype=core&format=json

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

30 September 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715635

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715635

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715635

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715635

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715635

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715635

A locus on chromosome 11p with multiple restriction site polymorphisms

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715635

Exomphalos-Macroglossia-Gigantism Syndrome in Jamaican Infants

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715635

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715635

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715635

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715635

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

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715635

An RFLP associated with the human catalase gene

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715635

Genomic imprinting and carcinogenesis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715635

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

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715635

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715635

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

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715635

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715635

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715635

Neoplasms associated with the Beckwith-Wiedemann syndrome

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715635

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715635

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

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715635

Strategies for multilocus linkage analysis in humans

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715635

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=1715635

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

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715635

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

26 September 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Loss of a Harvey ras allele in sporadic Wilms' tumour

1 reference

12 December 2020

Localization of the polymorphic human calcitonin gene on chromosome 11

1 reference

12 December 2020

Restriction fragment length polymorphisms at the human parathyroid hormone gene locus

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Degree of methylation of transgenes is dependent on gamete of origin

1 reference

12 December 2020

Chromosomal localization of the human rhabdomyosarcoma locus by mitotic recombination mapping

1 reference

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2539717%20AND%20SRC:MED&resulttype=core&format=json

30 September 2019

1 reference