(Q52093151)

English

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

scientific article published in January 1984

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Statements

scholarly article

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6745943

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

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6745943

author name string

C Turleau

1

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6745943

J de Grouchy

2

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6745943

F Chavin-Colin

3

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6745943

H Martelli

4

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6745943

M Voyer

5

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6745943

R Charlas

6

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6745943

publication date

1 January 1984

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6745943

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6745943

67

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6745943

219-221

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6745943

2

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6745943

https://scigraph.springernature.com/pub.10.1007/bf00273006

0 references

Partial trisomy of chromosome 11: a case report

1 reference

https://pubmed.ncbi.nlm.nih.gov/6745943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/6745943

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/6745943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/6745943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human gene mapping 7. Los Angeles conference (1983), Seventh International Workshop on Human Gene Mapping

1 reference

https://pubmed.ncbi.nlm.nih.gov/6745943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00273006

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6745943

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6745943

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