(Q50503844)

14 March 2018

title

Clinical and morphological features of Waardenburg syndrome type II. (English)

1 reference

14 March 2018

author name string

Mullaney PB

1

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14 March 2018

Parsons MA

2

1 reference

14 March 2018

Weatherhead RG

3

1 reference

14 March 2018

Karcioglu ZA

4

1 reference

14 March 2018

publication date

1 January 1998

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14 March 2018

published in

Eye

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14 March 2018

volume

12 ( Pt 3a)

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14 March 2018

page(s)

353-357

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14 March 2018

https://scigraph.springernature.com/pub.10.1038/eye.1998.85

exact match

0 references

cites work

Heterogeneity in Waardenburg's syndrome. Report of a family with ocular albinism.

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1998.85

Waardenburg syndrome type II: phenotypic findings and diagnostic criteria

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1998.85

Melanocytes and iris color. Electron microscopic findings.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1998.85

Melanocytes and iris color. Light microscopic findings.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1998.85

The fine structure of melanocytes in the human iris

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1998.85

Congenital Horner's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1998.85

An electron microscopic study of the iris stroma in monkey and rabbit with particular reference to intercellular contacts and sympathetic innervation of anterior layer cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1998.85

Innervation of melanocytes in human iris. An electron microscopic study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1998.85

Horner's syndrome: an electron microscopic study of a human iris

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1998.85

Piebaldism, Waardenburg syndrome, and related disorders of melanocyte development

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1998.85

Deafness as part of an hereditary syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1998.85

A novel mutation in the MITF gene causes Waardenburg Syndrome Type 2

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1998.85

Iris colour and relationship of tyrosinase activity to adrenergic innervation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1998.85

Waardenburg syndrome, Hirschsprung megacolon, and Marcus Gunn ptosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1998.85

7 January 2021

Waardenburg's syndrome with fundus and other anomalies

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1998.85

7 January 2021

Waardenburg'ssyndrome during the first year of life

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1998.85

7 January 2021

Innervation of iridic melanophores

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1998.85

7 January 2021

https://api.crossref.org/works/10.1038%2FEYE.1998.85

1 reference

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Origins of avian ocular and periocular tissues

1 reference

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7 January 2021

Identifiers

DOI

10.1038/EYE.1998.85

1 reference

14 March 2018

1 reference

14 March 2018