(Q77566826)

English

[Molecular diagnosis of mutations responsible for recurrent and severe forms of primary congenital glaucoma]

scientific article published on 01 January 1998

In more languages

edit

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9818478

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9818478%20AND%20SRC:MED&resulttype=core&format=json

retrieved

6 December 2019

title

[Molecular diagnosis of mutations responsible for recurrent and severe forms of primary congenital glaucoma] (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9818478

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9818478%20AND%20SRC:MED&resulttype=core&format=json

retrieved

6 December 2019

main subject

primary congenital glaucoma

1 reference

M Plásilová

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9818478

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9818478%20AND%20SRC:MED&resulttype=core&format=json

retrieved

6 December 2019

A Gerinec

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9818478

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9818478%20AND%20SRC:MED&resulttype=core&format=json

retrieved

6 December 2019

V Ferák

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9818478

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9818478%20AND%20SRC:MED&resulttype=core&format=json

retrieved

6 December 2019

publication date

1 January 1998

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9818478

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9818478%20AND%20SRC:MED&resulttype=core&format=json

retrieved

6 December 2019

published in

Ceska a slovenska oftalmologie : casopis Ceske oftalmologicke spolecnosti a Slovenske oftalmologicke spolecnosti

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9818478

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9818478%20AND%20SRC:MED&resulttype=core&format=json

retrieved

6 December 2019

volume

54

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9818478

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9818478%20AND%20SRC:MED&resulttype=core&format=json

retrieved

6 December 2019

issue

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9818478

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9818478%20AND%20SRC:MED&resulttype=core&format=json

retrieved

6 December 2019

page(s)

281-288

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9818478

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9818478%20AND%20SRC:MED&resulttype=core&format=json

retrieved

6 December 2019

Identifiers

PubMed publication ID

9818478

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9818478

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9818478%20AND%20SRC:MED&resulttype=core&format=json

(Q77566826)

[Molecular diagnosis of mutations responsible for recurrent and severe forms of primary congenital glaucoma]

Statements

Identifiers

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)