(Q54457712)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19852579%20AND%20SRC:MED&resulttype=core&format=json

10 February 2020

title

Mutations in KIF21A and PHOX2A are absent in 16 patients with congenital vertical incomitant strabismus (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19852579%20AND%20SRC:MED&resulttype=core&format=json

10 February 2020

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19852579%20AND%20SRC:MED&resulttype=core&format=json

10 February 2020

author name string

Arif O Khan

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19852579%20AND%20SRC:MED&resulttype=core&format=json

10 February 2020

Dania S Khalil

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19852579%20AND%20SRC:MED&resulttype=core&format=json

10 February 2020

Latifa J Al-Sharif

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19852579%20AND%20SRC:MED&resulttype=core&format=json

10 February 2020

publication date

1 December 2009

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19852579%20AND%20SRC:MED&resulttype=core&format=json

10 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19852579%20AND%20SRC:MED&resulttype=core&format=json

10 February 2020

volume

30

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19852579%20AND%20SRC:MED&resulttype=core&format=json

10 February 2020

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19852579%20AND%20SRC:MED&resulttype=core&format=json

10 February 2020

page(s)

206-207

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19852579%20AND%20SRC:MED&resulttype=core&format=json

110th ENMC International Workshop: the congenital cranial dysinnervation disorders (CCDDs). Naarden, The Netherlands, 25-27 October, 2002.

10 February 2020

cites work

1 reference

Crossref

https://api.crossref.org/works/10.3109%2F13816810903183613

Familial unilateral Brown syndrome

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.3109%2F13816810903183613

ARIX gene polymorphisms in patients with congenital superior oblique muscle palsy

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.3109%2F13816810903183613

10.3109/13816810903183613

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19852579%20AND%20SRC:MED&resulttype=core&format=json

10 February 2020

1 reference