(Q36771391)

16 August 2017

1 reference

title

Waardenburg's syndrome and familial periodic paralysis (English)

1 reference

16 August 2017

Waardenburg's syndrome

1 reference

1 reference

Tay CH

1

1 reference

PMC publication ID

2466925

16 August 2017

language of work or name

English

0 references

publication date

1 June 1971

1 reference

Postgraduate Medical Journal

16 August 2017

1 reference

16 August 2017

47

1 reference

16 August 2017

548

1 reference

16 August 2017

354-360

1 reference

A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root with pigmentary defects of the iris and head hair and with congenital deafness

16 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2466925

Studies in disorders of muscle. VII. Clinical manifestations and inheritance of a type of periodic paralysis without hypopotassemia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2466925

An English family with Waardenburg's syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2466925

Deafness as part of an hereditary syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2466925

A new form of congenital hereditary deafness (Waardenburg's syndrome).

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2466925

A Chinese family with Waardenburg's syndrome.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2466925

Periodic paralysis associated with hyperthyroidism: report of three cases

27 June 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/5580938

12 December 2020

Thyroid function and periodic paralysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/5580938

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/5580938

12 December 2020

Waardenbrug's syndrome. A variation of the first arch syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/5580938

12 December 2020

Identifiers

DOI

10.1136/PGMJ.47.548.354

1 reference

16 August 2017

1 reference

PMC publication ID

2466925

16 August 2017

PubMed publication ID

5580938

1 reference

PMC publication ID

2466925