(Q70878663)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7264803%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

title

White forelock, pigmentary disorder of irides, and long segment Hirschsprung disease: possible variant of Waardenburg syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7264803%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

White forelock, pigmentary disorder of irides, and long segment Hirschsprung disease: Possible variant of Waardenburg syndrome (English)

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(81)80339-3

5 April 2024

author name string

K. N. Shah

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7264803

5 April 2024

S. J. Dalal

2

1 reference

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5 April 2024

M. P. Desai

3

1 reference

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5 April 2024

P. N. Sheth

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7264803

5 April 2024

N. C. Joshi

5

1 reference

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5 April 2024

L. M. Ambani

6

1 reference

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5 April 2024

language of work or name

English

0 references

publication date

1 September 1981

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7264803%20AND%20SRC:MED&resulttype=core&format=json

full work available at URL

14 October 2019

https://api.elsevier.com/content/article/PII:S0022347681803393?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(81)80339-3

https://api.elsevier.com/content/article/PII:S0022347681803393?httpAccept=text/plain

5 April 2024

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(81)80339-3

The Journal of Pediatrics

5 April 2024

published in

1 reference

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14 October 2019

volume

99

1 reference

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14 October 2019

issue

3

1 reference

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14 October 2019

page(s)

432-435

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7264803%20AND%20SRC:MED&resulttype=core&format=json

Partial albinism and deaf-mutism due to a recessive sex-linked gene

14 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2881%2980339-3

The association of Waardenburg syndrome and Hirschsprung megacolon

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2881%2980339-3

Studies on megacolon in piebald mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2881%2980339-3

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2881%2980339-3

Heterogeneity in Waardenburg syndrome

7 January 2021

7

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(81)80339-3

5 April 2024

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7264803%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

1 reference