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9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia (32)
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Display all abstracts in classification 9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia
Search within classification 9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia74503 Axenfeld-Rieger syndrome
Seifi M
Clinical Genetics 2018; 93: 1123-1130
74740 Corneal Abnormalities in Congenital Aniridia: Congenital Central Corneal Opacity Versus Aniridia-associated Keratopathy
Lee HK
American Journal of Ophthalmology 2018; 185: 75-80
74371 Diagnostic impact of anterior segment angiography of limbal stem cell insufficiency in PAX6 related aniridia
Käsmann-Kellner B
Clinical anatomy (New York, N.Y.) 2018; 31: 392-397
74410 The genetics of congenital aniridia-a guide for the ophthalmologist
Landsend ES
Survey of Ophthalmology 2018; 63: 105-113
74739 4q25 microdeletion encompassing PITX2: A patient presenting with tetralogy of Fallot and dental anomalies without ocular features
Vande Perre P
European Journal of Medical Genetics 2018; 61: 72-78
74528 A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations
Khalil A
Frontiers in cardiovascular medicine 2017; 4: 58
74503 Axenfeld-Rieger syndrome
Walter MA
Clinical Genetics 2018; 93: 1123-1130
74371 Diagnostic impact of anterior segment angiography of limbal stem cell insufficiency in PAX6 related aniridia
Latta L
Clinical anatomy (New York, N.Y.) 2018; 31: 392-397
74410 The genetics of congenital aniridia-a guide for the ophthalmologist
Utheim ØA
Survey of Ophthalmology 2018; 63: 105-113
74739 4q25 microdeletion encompassing PITX2: A patient presenting with tetralogy of Fallot and dental anomalies without ocular features
Zazo Seco C
European Journal of Medical Genetics 2018; 61: 72-78
74528 A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations
Al-Haddad C
Frontiers in cardiovascular medicine 2017; 4: 58
74740 Corneal Abnormalities in Congenital Aniridia: Congenital Central Corneal Opacity Versus Aniridia-associated Keratopathy
Kim MK
American Journal of Ophthalmology 2018; 185: 75-80
74371 Diagnostic impact of anterior segment angiography of limbal stem cell insufficiency in PAX6 related aniridia
Fries F
Clinical anatomy (New York, N.Y.) 2018; 31: 392-397
74410 The genetics of congenital aniridia-a guide for the ophthalmologist
Pedersen HR
Survey of Ophthalmology 2018; 63: 105-113
74740 Corneal Abnormalities in Congenital Aniridia: Congenital Central Corneal Opacity Versus Aniridia-associated Keratopathy
Oh JY
American Journal of Ophthalmology 2018; 185: 75-80
74739 4q25 microdeletion encompassing PITX2: A patient presenting with tetralogy of Fallot and dental anomalies without ocular features
Patat O
European Journal of Medical Genetics 2018; 61: 72-78
74528 A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations
Hariri H
Frontiers in cardiovascular medicine 2017; 4: 58
74739 4q25 microdeletion encompassing PITX2: A patient presenting with tetralogy of Fallot and dental anomalies without ocular features
Bouneau L
European Journal of Medical Genetics 2018; 61: 72-78
74528 A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations
Shibbani K
Frontiers in cardiovascular medicine 2017; 4: 58
74410 The genetics of congenital aniridia-a guide for the ophthalmologist
Lagali N
Survey of Ophthalmology 2018; 63: 105-113
74371 Diagnostic impact of anterior segment angiography of limbal stem cell insufficiency in PAX6 related aniridia
Viestenz A
Clinical anatomy (New York, N.Y.) 2018; 31: 392-397
74410 The genetics of congenital aniridia-a guide for the ophthalmologist
Baraas RC
Survey of Ophthalmology 2018; 63: 105-113
74739 4q25 microdeletion encompassing PITX2: A patient presenting with tetralogy of Fallot and dental anomalies without ocular features
Vigouroux A
European Journal of Medical Genetics 2018; 61: 72-78
74528 A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations
Bitar F
Frontiers in cardiovascular medicine 2017; 4: 58
74371 Diagnostic impact of anterior segment angiography of limbal stem cell insufficiency in PAX6 related aniridia
Seitz B
Clinical anatomy (New York, N.Y.) 2018; 31: 392-397
