(Q52029788)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16389592%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

title

A novel homeobox mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome associated with brain, ocular, and dental phenotypes (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16389592%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

main subject

Axenfeld-Rieger syndrome

1 reference

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16389592%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

Jane Sowden

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16389592%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

5

Pamela J Thompson

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16389592%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

8

Paul Rutland

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16389592%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

Maria Bitner-Glindzicz

9

object named as

Maria Bitner-Glindzicz

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16389592%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

author name string

Faisal Idrees

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16389592%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

Samantha L Free

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16389592%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

Daniela Vaideanu

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16389592%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

Paul Ashley

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16389592%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

Glen Brice

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16389592%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

Peng T Khaw

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16389592%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

Scott Fraser

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16389592%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

Sanjay M Sisodiya

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16389592%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

publication date

1 March 2006

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16389592%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

15 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16389592%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

volume

141B

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16389592%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16389592%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

page(s)

184-191

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16389592%20AND%20SRC:MED&resulttype=core&format=json

Chromosomal duplication involving the forkhead transcription factor gene FOXC1 causes iris hypoplasia and glaucoma

15 January 2020

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FAJMG.B.30237

Cognitive functioning in humans with mutations of the PAX6 gene.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FAJMG.B.30237