(Q52222774)

English

Tight linkage between the Beckwith-Wiedemann syndrome and a microsatellite marker for the TH locus.

scientific article published in October 1993

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scholarly article

1 reference

Europe PubMed Central

27 April 2018

http://europepmc.org/abstract/MED/8104862

Tight linkage between the Beckwith-Wiedemann syndrome and a microsatellite marker for the TH locus. (English)

1 reference

Europe PubMed Central

27 April 2018

http://europepmc.org/abstract/MED/8104862

1 reference

based on heuristic

inferred from title

Beckwith-Wiedemann syndrome

1 reference

based on heuristic

inferred from title

Agneta Nordenskjöld

object named as

A Nordenskjöld

1

0 references

Magnus Nordenskjöld

object named as

M Nordenskjöld

4

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author name string

F Hedborg

2

1 reference

Europe PubMed Central

27 April 2018

http://europepmc.org/abstract/MED/8104862

H Luthman

3

1 reference

Europe PubMed Central

27 April 2018

http://europepmc.org/abstract/MED/8104862

publication date

1 October 1993

1 reference

Europe PubMed Central

27 April 2018

http://europepmc.org/abstract/MED/8104862

1 reference

Europe PubMed Central

27 April 2018

http://europepmc.org/abstract/MED/8104862

92

1 reference

Europe PubMed Central

27 April 2018

http://europepmc.org/abstract/MED/8104862

296-298

1 reference

Europe PubMed Central

27 April 2018

http://europepmc.org/abstract/MED/8104862

3

1 reference

Europe PubMed Central

27 April 2018

http://europepmc.org/abstract/MED/8104862

https://scigraph.springernature.com/pub.10.1007/bf00244475

0 references

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8104862

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic variation at five trimeric and tetrameric tandem repeat loci in four human population groups

1 reference

https://pubmed.ncbi.nlm.nih.gov/8104862

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human tyrosine hydroxylase and insulin genes are contiguous on chromosome 11

1 reference

https://pubmed.ncbi.nlm.nih.gov/8104862

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Uniparental paternal disomy in a genetic cancer-predisposing syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8104862

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8104862

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Beckwith-Wiedemann syndrome: a demonstration of the mechanisms responsible for the excess of transmitting females

1 reference

https://pubmed.ncbi.nlm.nih.gov/8104862

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Beckwith-wiedemann syndrome and neural crest tumors. A report of two cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/8104862

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic linkage of Beckwith-Wiedemann syndrome to 11p15.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8104862

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neoplasms associated with the Beckwith-Wiedemann syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8104862

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nephrogenic rests, nephroblastomatosis, and the pathogenesis of Wilms' tumor

1 reference

https://pubmed.ncbi.nlm.nih.gov/8104862

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tetranucleotide repeat polymorphism at the human tyrosine hydroxylase gene (TH).

1 reference

https://pubmed.ncbi.nlm.nih.gov/8104862

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complete and incomplete forms of Beckwith-Wiedemann syndrome: their oncogenic potential

1 reference

https://pubmed.ncbi.nlm.nih.gov/8104862

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neuroblastoma associated with Beckwith-Wiedemann syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8104862

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction

1 reference

https://pubmed.ncbi.nlm.nih.gov/8104862

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital pancreatoblastoma in Beckwith-Wiedemann syndrome: an emerging association

1 reference

https://pubmed.ncbi.nlm.nih.gov/8104862

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Beckwith-Wiedemann syndrome, tumourigenesis and imprinting

1 reference

https://pubmed.ncbi.nlm.nih.gov/8104862

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for paternal imprinting in familial Beckwith-Wiedemann syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8104862

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00244475

1 reference

Europe PubMed Central

27 April 2018

http://europepmc.org/abstract/MED/8104862

1 reference

Europe PubMed Central

27 April 2018

http://europepmc.org/abstract/MED/8104862

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