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9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia (17)

Showing records 1 to 17

Display all abstracts in classification 9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia

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69038 Unilateral persistent fetal vasculature coexisting with anterior segment dysgenesia
Cañizares B
Archivos de la Sociedad Española de Oftalmologia 2017; 92: 40-43

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69441 Conditional deletion of AP-2β in mouse cranial neural crest results in anterior segment dysgenesis and early-onset glaucoma
Martino VB
Disease models & mechanisms 2016; 9: 849-861

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69406 A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
Micheal S
PLoS ONE 2016; 11: e0160016

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69038 Unilateral persistent fetal vasculature coexisting with anterior segment dysgenesia
Yago I
Archivos de la Sociedad Española de Oftalmologia 2017; 92: 40-43

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69441 Conditional deletion of AP-2β in mouse cranial neural crest results in anterior segment dysgenesis and early-onset glaucoma
Sabljic T
Disease models & mechanisms 2016; 9: 849-861

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69406 A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
Siddiqui SN
PLoS ONE 2016; 11: e0160016

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69441 Conditional deletion of AP-2β in mouse cranial neural crest results in anterior segment dysgenesis and early-onset glaucoma
Deschamps P
Disease models & mechanisms 2016; 9: 849-861

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69038 Unilateral persistent fetal vasculature coexisting with anterior segment dysgenesia
Piñero Á
Archivos de la Sociedad Española de Oftalmologia 2017; 92: 40-43

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69406 A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
Zafar SN; Villanueva-Mendoza C
PLoS ONE 2016; 11: e0160016

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69441 Conditional deletion of AP-2β in mouse cranial neural crest results in anterior segment dysgenesis and early-onset glaucoma
Green RM
Disease models & mechanisms 2016; 9: 849-861

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69038 Unilateral persistent fetal vasculature coexisting with anterior segment dysgenesia
Ruiz M
Archivos de la Sociedad Española de Oftalmologia 2017; 92: 40-43

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69406 A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
Cortés-González V
PLoS ONE 2016; 11: e0160016

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69441 Conditional deletion of AP-2β in mouse cranial neural crest results in anterior segment dysgenesis and early-onset glaucoma
Akula M; Peacock E
Disease models & mechanisms 2016; 9: 849-861

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69406 A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
Khan MI
PLoS ONE 2016; 11: e0160016

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69441 Conditional deletion of AP-2β in mouse cranial neural crest results in anterior segment dysgenesis and early-onset glaucoma
Ball A
Disease models & mechanisms 2016; 9: 849-861

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69406 A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
den Hollander AI
PLoS ONE 2016; 11: e0160016

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69441 Conditional deletion of AP-2β in mouse cranial neural crest results in anterior segment dysgenesis and early-onset glaucoma
Williams T; West-Mays JA
Disease models & mechanisms 2016; 9: 849-861

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