Case of novel PITX2 gene mutation associated with Peters' anomaly and persistent hyperplastic primary vitreous. (Q47746506)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19461663%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

title

Case of novel PITX2 gene mutation associated with Peters' anomaly and persistent hyperplastic primary vitreous (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19461663%20AND%20SRC:MED&resulttype=core&format=json

persistent fetal vasculature

28 January 2020

main subject

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author

Shigeo Yoshida

2

1 reference

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28 January 2020

author name string

A Arikawa

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19461663%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

H Yoshikawa

3

1 reference

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28 January 2020

K Ishikawa

4

1 reference

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28 January 2020

Y Yamaji

5

1 reference

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28 January 2020

R-I Arita

6

1 reference

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28 January 2020

A Ueno

7

1 reference

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28 January 2020

T Ishibashi

8

1 reference

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28 January 2020

publication date

22 May 2009

1 reference

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28 January 2020

1 reference

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28 January 2020

volume

24

1 reference

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28 January 2020

issue

2

1 reference

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28 January 2020

page(s)

391-393

1 reference

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https://scigraph.springernature.com/pub.10.1038/eye.2009.114

28 January 2020

exact match

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cites work

Case of chromosome 6p25 terminal deletion associated with Axenfeld-Rieger syndrome and persistent hyperplastic primary vitreous

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.114

Histopathological examination of two cases of anterior staphyloma associated with Peters' anomaly and persistent hyperplastic primary vitreous

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.114

inferred from DOI database lookup

7 January 2021

based on heuristic

Expression of the homeobox gene Pitx2 in neural crest is required for optic stalk and ocular anterior segment development.

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.114

inferred from DOI database lookup

7 January 2021

based on heuristic

Functional interactions between FOXC1 and PITX2 underlie the sensitivity to FOXC1 gene dose in Axenfeld-Rieger syndrome and anterior segment dysgenesis

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.114