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9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia (34)
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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, aniridia60487 Anirdia-like phenotype caused by 6p25 dosage aberrations
Sadagopan KA
American Journal of Medical Genetics, Part A 2015; 167: 524-528
60492 A novel splice site mutation in the PAX6 gene in a Korean family with isolated aniridia
Chang MS
Annals of clinical and laboratory science 2015; 45: 90-93
60462 Mutational analysis and genotype-phenotype correlations in southern Indian patients with sporadic and familial aniridia
Dubey SK
Molecular Vision 2015; 21: 88-97
60059 Aniridia syndrome: clinical findings, problematic courses and suggestions for optimization of care ("aniridia guide")
Käsmann-Kellner B
Ophthalmologe 2014; 111: 1145-1156
60579 Ultrasound biomicroscopy in infants with congenital corneal opacity and its correlations with clinical diagnosis and intraocular pressure
Yoshikawa H
Nippon Ganka Gakkai Zasshi 2015; 119: 16-21
60118 Functional Analysis of FOXE3 Mutations Causing Dominant and Recessive Ocular Anterior Segment Disease
Islam L
Human Mutation 2015; 36: 296-300
60060 Stage-related therapy of congenital aniridia
Seitz B
Ophthalmologe 2014; 111: 1164-1171
60579 Ultrasound biomicroscopy in infants with congenital corneal opacity and its correlations with clinical diagnosis and intraocular pressure
Ikeda Y
Nippon Ganka Gakkai Zasshi 2015; 119: 16-21
60462 Mutational analysis and genotype-phenotype correlations in southern Indian patients with sporadic and familial aniridia
Mahalaxmi N
Molecular Vision 2015; 21: 88-97
60118 Functional Analysis of FOXE3 Mutations Causing Dominant and Recessive Ocular Anterior Segment Disease
Kelberman D
Human Mutation 2015; 36: 296-300
60492 A novel splice site mutation in the PAX6 gene in a Korean family with isolated aniridia
Han JC
Annals of clinical and laboratory science 2015; 45: 90-93
60487 Anirdia-like phenotype caused by 6p25 dosage aberrations
Liu GT
American Journal of Medical Genetics, Part A 2015; 167: 524-528
60060 Stage-related therapy of congenital aniridia
Käsmann-Kellner B
Ophthalmologe 2014; 111: 1164-1171
60059 Aniridia syndrome: clinical findings, problematic courses and suggestions for optimization of care ("aniridia guide")
Seitz B
Ophthalmologe 2014; 111: 1145-1156
60060 Stage-related therapy of congenital aniridia
Viestenz A
Ophthalmologe 2014; 111: 1164-1171
60579 Ultrasound biomicroscopy in infants with congenital corneal opacity and its correlations with clinical diagnosis and intraocular pressure
Sotozono C
Nippon Ganka Gakkai Zasshi 2015; 119: 16-21
60118 Functional Analysis of FOXE3 Mutations Causing Dominant and Recessive Ocular Anterior Segment Disease
Williamson L
Human Mutation 2015; 36: 296-300
60492 A novel splice site mutation in the PAX6 gene in a Korean family with isolated aniridia
Lee J
Annals of clinical and laboratory science 2015; 45: 90-93
60462 Mutational analysis and genotype-phenotype correlations in southern Indian patients with sporadic and familial aniridia
Vijayalakshmi P
Molecular Vision 2015; 21: 88-97
60487 Anirdia-like phenotype caused by 6p25 dosage aberrations
Capasso JE; Wuthisiri W
American Journal of Medical Genetics, Part A 2015; 167: 524-528
60492 A novel splice site mutation in the PAX6 gene in a Korean family with isolated aniridia
Kwun Y
Annals of clinical and laboratory science 2015; 45: 90-93
60118 Functional Analysis of FOXE3 Mutations Causing Dominant and Recessive Ocular Anterior Segment Disease
Lewis N
Human Mutation 2015; 36: 296-300
60579 Ultrasound biomicroscopy in infants with congenital corneal opacity and its correlations with clinical diagnosis and intraocular pressure
Mori K
Nippon Ganka Gakkai Zasshi 2015; 119: 16-21
60462 Mutational analysis and genotype-phenotype correlations in southern Indian patients with sporadic and familial aniridia
Sundaresan P
Molecular Vision 2015; 21: 88-97
60487 Anirdia-like phenotype caused by 6p25 dosage aberrations
Keep RB
American Journal of Medical Genetics, Part A 2015; 167: 524-528