(Q78920181)

English

Waardenburg's syndrome. A syndrome of heterochromia of the irides, lateral displacement of the medial canthi and lacrimal puncta, congenital deafness, and other characteristic associated defects

scientific article published on 01 November 1960

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13722846%20AND%20SRC:MED&resulttype=core&format=json

17 December 2019

Waardenburg's syndrome. A syndrome of heterochromia of the irides, lateral displacement of the medial canthi and lacrimal puncta, congenital deafness, and other characteristic associated defects (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13722846%20AND%20SRC:MED&resulttype=core&format=json

17 December 2019

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A M DIGEORGE

1

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13722846%20AND%20SRC:MED&resulttype=core&format=json

17 December 2019

R W OLMSTED

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13722846%20AND%20SRC:MED&resulttype=core&format=json

17 December 2019

R D HARLEY

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13722846%20AND%20SRC:MED&resulttype=core&format=json

17 December 2019

publication date

1 November 1960

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13722846%20AND%20SRC:MED&resulttype=core&format=json

17 December 2019

The Journal of Pediatrics

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13722846%20AND%20SRC:MED&resulttype=core&format=json

17 December 2019

57

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13722846%20AND%20SRC:MED&resulttype=core&format=json

17 December 2019

649-669

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13722846%20AND%20SRC:MED&resulttype=core&format=json

17 December 2019

The first arch syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2860%2980159-X

7 January 2021

An English family with Waardenburg's syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2860%2980159-X

7 January 2021

Deafness as part of an hereditary syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2860%2980159-X

7 January 2021

Congenital deafness in white cats.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2860%2980159-X

7 January 2021

Identifiers

10.1016/S0022-3476(60)80159-X

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13722846%20AND%20SRC:MED&resulttype=core&format=json

17 December 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13722846%20AND%20SRC:MED&resulttype=core&format=json

17 December 2019

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