(Q37340744)

19 August 2017

Waardenburg's syndrome. Report of a family (English)

1 reference

19 August 2017

Cant JS

1

1 reference

19 August 2017

Martin AJ

series ordinal

2

1 reference

19 August 2017

language of work or name

English

0 references

publication date

1 November 1967

1 reference

British Journal of Ophthalmology

19 August 2017

1 reference

19 August 2017

51

1 reference

19 August 2017

11

1 reference

19 August 2017

755-759

1 reference

WAARDENBURG'S SYNDROME AND HETEROCHROMIA IRIDUM IN A DEAF SCHOOL POPULATION

19 August 2017

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=506489

Deafness as part of an hereditary syndrome

6 September 2017

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=506489

Waardenburg's syndrome in father and daughter

26 June 2018

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=506489

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

2 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/6060805

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Waardenburg's syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/6060805

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/BJO.51.11.755

1 reference

19 August 2017

1 reference

19 August 2017

PubMed publication ID

6060805

1 reference