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

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

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80790 Ocular bleeding in an undiagnosed hemophiliac neonate causing irreversible loss of vision: A case report with review of the literature
Al-Sharif E
European Journal of Ophthalmology 2019; 0: 1120672119841188
81244 A novel frameshift mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome using targeted exome sequencing
Zhang L
BMC Medical Genetics 2019; 20: 105
80982 Glaucoma Surgery in Anterior Segment Dysgeneses
van Oterendorp C
Klinische Monatsblätter für Augenheilkunde 2019; 236: 745-750
81362 Glaucoma Management in Patients with Aniridia and Boston Type 1 Keratoprosthesis
Nascimento E Silva R
American Journal of Ophthalmology 2019; 207: 258-267
81244 A novel frameshift mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome using targeted exome sequencing
Peng Y
BMC Medical Genetics 2019; 20: 105
80790 Ocular bleeding in an undiagnosed hemophiliac neonate causing irreversible loss of vision: A case report with review of the literature
AlEnezi SH
European Journal of Ophthalmology 2019; 0: 1120672119841188
81362 Glaucoma Management in Patients with Aniridia and Boston Type 1 Keratoprosthesis
Shen LQ; Chiou CA
American Journal of Ophthalmology 2019; 207: 258-267
81244 A novel frameshift mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome using targeted exome sequencing
Ouyang P
BMC Medical Genetics 2019; 20: 105
80790 Ocular bleeding in an undiagnosed hemophiliac neonate causing irreversible loss of vision: A case report with review of the literature
Sharif HA
European Journal of Ophthalmology 2019; 0: 1120672119841188
81362 Glaucoma Management in Patients with Aniridia and Boston Type 1 Keratoprosthesis
Shanbhag SS
American Journal of Ophthalmology 2019; 207: 258-267
80790 Ocular bleeding in an undiagnosed hemophiliac neonate causing irreversible loss of vision: A case report with review of the literature
Osman EA
European Journal of Ophthalmology 2019; 0: 1120672119841188
81244 A novel frameshift mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome using targeted exome sequencing
Liang Y; Zeng H
BMC Medical Genetics 2019; 20: 105
81362 Glaucoma Management in Patients with Aniridia and Boston Type 1 Keratoprosthesis
Paschalis EI; Pasquale LR
American Journal of Ophthalmology 2019; 207: 258-267
81244 A novel frameshift mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome using targeted exome sequencing
Wang N; Duan X
BMC Medical Genetics 2019; 20: 105
81362 Glaucoma Management in Patients with Aniridia and Boston Type 1 Keratoprosthesis
Colby KA
American Journal of Ophthalmology 2019; 207: 258-267
81244 A novel frameshift mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome using targeted exome sequencing
Shi J
BMC Medical Genetics 2019; 20: 105
81362 Glaucoma Management in Patients with Aniridia and Boston Type 1 Keratoprosthesis
Dohlman CH; Chodosh J; Alves MR
American Journal of Ophthalmology 2019; 207: 258-267

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