(Q24322057)

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Autosomal dominant iris hypoplasia is caused by a mutation in the Rieger syndrome (RIEG/PITX2) gene

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title

Autosomal dominant iris hypoplasia is caused by a mutation in the Rieger syndrome (RIEG/PITX2) gene (English)

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main subject

Paired like homeodomain 2

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stated in

GOA release 2020-03-11

iris morphogenesis

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stated in

GOA release 2020-03-11

author name string

W L Alward

series ordinal

1

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E V Semina

series ordinal

2

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J W Kalenak

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3

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E Héon

series ordinal

4

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B P Sheth

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5

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E M Stone

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6

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J C Murray

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7

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language of work or name

English

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publication date

January 1998

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published in

American Journal of Ophthalmology

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volume

125

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issue

1

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page(s)

98-100

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cites work

Familial glaucoma. In nine generations of a South Hampshire family

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reference URL

https://api.crossref.org/works/10.1016%2FS0002-9394%2899%2980242-6

retrieved

7 January 2021

Linkage of autosomal dominant iris hypoplasia to the region of the Rieger syndrome locus (4q25)

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Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0002-9394%2899%2980242-6

retrieved

7 January 2021

Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0002-9394%2899%2980242-6

retrieved

7 January 2021

Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome

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Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0002-9394%2899%2980242-6

retrieved

7 January 2021

Genetic clues to glaucoma's secrets. The L Edward Jackson Memorial Lecture. Part 2.

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reference URL

https://api.crossref.org/works/10.1016%2FS0002-9394%2899%2980242-6

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7 January 2021

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DOI

10.1016/S0002-9394(99)80242-6

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stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1835626

OpenCitations bibliographic resource ID

1835626

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stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1835626

(Q24322057)

Autosomal dominant iris hypoplasia is caused by a mutation in the Rieger syndrome (RIEG/PITX2) gene

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