(Q33743894)

29 July 2017

0 references

Dental and Craniofacial Anomalies Associated with Axenfeld-Rieger Syndrome with PITX2 Mutation (English)

1 reference

29 July 2017

main subject

Axenfeld-Rieger syndrome

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inferred from title

author

Anahita Jablonski-Momeni

4

object named as

Anahita Jablonski-Momeni

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author name string

Simone Dressler

1

1 reference

29 July 2017

Philipp Meyer-Marcotty

2

1 reference

29 July 2017

Nicole Weisschuh

3

1 reference

29 July 2017

Klaus Pieper

5

1 reference

29 July 2017

Gwendolyn Gramer

6

1 reference

29 July 2017

Eugen Gramer

7

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29 July 2017

publication date

21 March 2010

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29 July 2017

published in

Case Reports in Medicine

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29 July 2017

volume

2010

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29 July 2017

page(s)

621984

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Creative Commons Attribution 3.0 Unported

29 July 2017

copyright license

start time

1 January 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

1 reference

April 2022 Public Data File from Crossref

cites work

Morphology of the sella turcica in Axenfeld-Rieger syndrome with PITX2 mutation

1 reference

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Dental anomalies in Axenfeld-Rieger syndrome.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2842968

Antagonistic regulation of Dlx2 expression by PITX2 and Msx2: implications for tooth development

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2842968

Identification of a dominant negative homeodomain mutation in Rieger syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2842968

Axenfeld-Rieger syndrome in the age of molecular genetics

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2842968

Atrial septal defect with interatrial aneurysm and Axenfeld-Rieger syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2842968

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2842968

Axenfeld-Rieger syndrome. A spectrum of developmental disorders

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2842968

Oral manifestations of the Rieger syndrome: report of case.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2842968

Anomalies associated with Axenfeld-Rieger syndrome.

14 July 2018

1 reference

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Novel mutations of FOXC1 and PITX2 in patients with Axenfeld-Rieger malformations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2010%2F621984

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

21 January 2018

1 reference

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A molecular basis for differential developmental anomalies in Axenfeld-Rieger syndrome

21 January 2018

1 reference

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The Rieger syndrome: orofacial manifestations. Case report of a rare condition.

21 January 2018

1 reference

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Variation in residual PITX2 activity underlies the phenotypic spectrum of anterior segment developmental disorders.

30 October 2018

1 reference

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Rieger's syndrome: a case report

30 October 2018

1 reference

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Four novel mutations in the PITX2 gene in patients with Axenfeld-Rieger syndrome

30 October 2018

1 reference

12 December 2020

[Morphology, family history, and age at diagnosis of 26 patients with Axenfeld-Rieger syndrome and glaucoma or ocular hypertension]

1 reference

12 December 2020

Dental and craniofacial anomalies of Axenfeld-Rieger syndrome

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12 December 2020

Rieger syndrome: a case report

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12 December 2020

Rieger syndrome is associated with PAX6 deletion

1 reference

12 December 2020

A meta-analysis of the prevalence of dental agenesis of permanent teeth

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12 December 2020

The Rieger anomaly concomitant with multiple dental, craniofacial, and somatic midline anomalies and short stature

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12 December 2020

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12 December 2020

[Missing upper incisors as cardinal symptom in Rieger's syndrome]

1 reference

12 December 2020

Identifiers

DOI

10.1155/2010/621984

1 reference

29 July 2017

1 reference

29 July 2017

1 reference