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9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia (19)
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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, aniridia81362 Glaucoma Management in Patients with Aniridia and Boston Type 1 Keratoprosthesis
Nascimento E Silva R
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
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
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
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
Sharif HA
European Journal of Ophthalmology 2019; 0: 1120672119841188
81362 Glaucoma Management in Patients with Aniridia and Boston Type 1 Keratoprosthesis
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
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
BMC Medical Genetics 2019; 20: 105
81362 Glaucoma Management in Patients with Aniridia and Boston Type 1 Keratoprosthesis
Shanbhag SS; Paschalis EI
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
Zeng H; Wang N
BMC Medical Genetics 2019; 20: 105
81362 Glaucoma Management in Patients with Aniridia and Boston Type 1 Keratoprosthesis
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
Duan X
BMC Medical Genetics 2019; 20: 105
81362 Glaucoma Management in Patients with Aniridia and Boston Type 1 Keratoprosthesis
Colby KA; Dohlman CH
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
Chodosh J; Alves MR
American Journal of Ophthalmology 2019; 207: 258-267
