(Q50602058)

English

Syndromes associated with congenital facial paralysis.

scientific article published in March 1981

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Europe PubMed Central

16 March 2018

http://europepmc.org/abstract/MED/6787538

title

Syndromes associated with congenital facial paralysis. (English)

1 reference

stated in

Europe PubMed Central

16 March 2018

http://europepmc.org/abstract/MED/6787538

author name string

L Bergstrom

series ordinal

1

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Europe PubMed Central

16 March 2018

http://europepmc.org/abstract/MED/6787538

B B Baker

series ordinal

2

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Europe PubMed Central

16 March 2018

http://europepmc.org/abstract/MED/6787538

publication date

1 March 1981

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Europe PubMed Central

16 March 2018

http://europepmc.org/abstract/MED/6787538

published in

Otolaryngology—Head and Neck Surgery

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stated in

Europe PubMed Central

16 March 2018

http://europepmc.org/abstract/MED/6787538

volume

89

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Europe PubMed Central

16 March 2018

http://europepmc.org/abstract/MED/6787538

page(s)

336-342

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Europe PubMed Central

16 March 2018

http://europepmc.org/abstract/MED/6787538

issue

2

1 reference

stated in

Europe PubMed Central

16 March 2018

http://europepmc.org/abstract/MED/6787538

cites work

Facial paralysis in children. A review of 150 cases

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1177%2F019459988108900238

retrieved

21 January 2018

Cardiofacial syndrome. Congenital heart disease and facial weakness, a hitherto unrecognized association

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Crossref

reference URL

https://api.crossref.org/works/10.1177%2F019459988108900238

retrieved

21 January 2018

Patterns of anomalies in children with malformed ears.

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Crossref

reference URL

https://api.crossref.org/works/10.1177%2F019459988108900238

retrieved

21 January 2018

Identifiers

DOI

10.1177/019459988108900238

1 reference

stated in

Europe PubMed Central

16 March 2018

http://europepmc.org/abstract/MED/6787538

PubMed ID

6787538

1 reference

stated in

Europe PubMed Central

16 March 2018

http://europepmc.org/abstract/MED/6787538

(Q50602058)

Syndromes associated with congenital facial paralysis.

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