Trisomy 11p15 and Beckwith-Wiedemann syndrome. A report of two cases. (Q52093151)

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scientific article published in January 1984

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English	Trisomy 11p15 and Beckwith-Wiedemann syndrome. A report of two cases.	scientific article published in January 1984

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scholarly article

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Europe PubMed Central

PubMed publication ID

6745943

retrieved

22 April 2018

reference URL

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

title

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

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Europe PubMed Central

PubMed publication ID

6745943

retrieved

22 April 2018

reference URL

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

author name string

C Turleau

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6745943

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22 April 2018

reference URL

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

J de Grouchy

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2

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Europe PubMed Central

PubMed publication ID

6745943

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22 April 2018

reference URL

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

F Chavin-Colin

series ordinal

3

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Europe PubMed Central

PubMed publication ID

6745943

retrieved

22 April 2018

reference URL

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

H Martelli

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4

1 reference

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Europe PubMed Central

PubMed publication ID

6745943

retrieved

22 April 2018

reference URL

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

M Voyer

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5

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Europe PubMed Central

PubMed publication ID

6745943

retrieved

22 April 2018

reference URL

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

R Charlas

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6

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stated in

Europe PubMed Central

PubMed publication ID

6745943

retrieved

22 April 2018

reference URL

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

publication date

1 January 1984

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Europe PubMed Central

PubMed publication ID

6745943

retrieved

22 April 2018

reference URL

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

published in

Human Genetics

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stated in

Europe PubMed Central

PubMed publication ID

6745943

retrieved

22 April 2018

reference URL

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

volume

67

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6745943

retrieved

22 April 2018

reference URL

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

issue

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6745943

retrieved

22 April 2018

reference URL

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

page(s)

219-221

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Europe PubMed Central

PubMed publication ID

6745943

retrieved

22 April 2018

reference URL

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

cites work

Partial trisomy of chromosome 11: a case report

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PubMed

reference URL

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

retrieved

12 December 2020

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

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PubMed

reference URL

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

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

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PubMed

reference URL

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

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

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PubMed

reference URL

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

retrieved

12 December 2020

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

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PubMed

reference URL

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

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12 December 2020

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Identifiers

DOI

10.1007/BF00273006

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stated in

Europe PubMed Central

PubMed publication ID

6745943

retrieved

22 April 2018

reference URL

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

PubMed publication ID

6745943

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6745943

retrieved

22 April 2018

reference URL

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

 

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