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

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

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title

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

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nephroblastoma

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Koufos A

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Grundy P

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Morgan K

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Aleck KA

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Hadro T

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Lampkin BC

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Kalbakji A

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Cavenee WK

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1 May 1989

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published in

American Journal of Human Genetics

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44

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5

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711-719

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

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https://pubmed.ncbi.nlm.nih.gov/2539717

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12 December 2020

based on heuristic

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

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reference URL

https://pubmed.ncbi.nlm.nih.gov/2539717

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12 December 2020

based on heuristic

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Loss of a Harvey ras allele in sporadic Wilms' tumour

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reference URL

https://pubmed.ncbi.nlm.nih.gov/2539717

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12 December 2020

based on heuristic

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Localization of the polymorphic human calcitonin gene on chromosome 11

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https://pubmed.ncbi.nlm.nih.gov/2539717

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12 December 2020

based on heuristic

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https://pubmed.ncbi.nlm.nih.gov/2539717

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based on heuristic

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

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https://pubmed.ncbi.nlm.nih.gov/2539717

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12 December 2020

based on heuristic

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

1 reference

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https://pubmed.ncbi.nlm.nih.gov/2539717

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12 December 2020

based on heuristic

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

1 reference

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https://pubmed.ncbi.nlm.nih.gov/2539717

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12 December 2020

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

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reference URL

https://pubmed.ncbi.nlm.nih.gov/2539717

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2539717

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2539717

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Degree of methylation of transgenes is dependent on gamete of origin

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2539717

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal localization of the human rhabdomyosarcoma locus by mitotic recombination mapping

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2539717

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2539717

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2539717

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2539717

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2539717

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2539717

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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1715635

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1715635

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2539717

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Europe PubMed Central

PMC publication ID

1715635

reference URL

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

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