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WGC-2021

9.4.4.5 Other (12)

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Display all abstracts in classification 9.4.4.5 Other

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80811 Phacolytic glaucoma: A nearly forgotten entity
Dhingra D
European Journal of Ophthalmology 2019; 0: 1120672119841972
80908 A novel nonsense mutation in ADAMTS17 caused autosomal recessive inheritance Weill-Marchesani syndrome from a Chinese family
Yi H
Journal of Human Genetics 2019; 64: 681-687
80811 Phacolytic glaucoma: A nearly forgotten entity
Dhingra D; Dhingra D
European Journal of Ophthalmology 2019; 0: 1120672119841972
81100 Large Capsulorhexis Related Uveitis-Glaucoma-Hyphema Syndrome Managed by Intraocular Lens Implant Exchange and Gonioscopy Assisted Transluminal Trabeculotomy
Razeghinejad MR
Journal of ophthalmic & vision research 2019; 14: 215-218
80908 A novel nonsense mutation in ADAMTS17 caused autosomal recessive inheritance Weill-Marchesani syndrome from a Chinese family
Zha X
Journal of Human Genetics 2019; 64: 681-687
81100 Large Capsulorhexis Related Uveitis-Glaucoma-Hyphema Syndrome Managed by Intraocular Lens Implant Exchange and Gonioscopy Assisted Transluminal Trabeculotomy
Havens SJ
Journal of ophthalmic & vision research 2019; 14: 215-218
80811 Phacolytic glaucoma: A nearly forgotten entity
Grover S
European Journal of Ophthalmology 2019; 0: 1120672119841972
80908 A novel nonsense mutation in ADAMTS17 caused autosomal recessive inheritance Weill-Marchesani syndrome from a Chinese family
Zhu Y
Journal of Human Genetics 2019; 64: 681-687
80811 Phacolytic glaucoma: A nearly forgotten entity
Kapatia G; Pandav SS
European Journal of Ophthalmology 2019; 0: 1120672119841972
80908 A novel nonsense mutation in ADAMTS17 caused autosomal recessive inheritance Weill-Marchesani syndrome from a Chinese family
Lv J
Journal of Human Genetics 2019; 64: 681-687
80811 Phacolytic glaucoma: A nearly forgotten entity
Kaushik S
European Journal of Ophthalmology 2019; 0: 1120672119841972
80908 A novel nonsense mutation in ADAMTS17 caused autosomal recessive inheritance Weill-Marchesani syndrome from a Chinese family
Hu S; Kong Y; Wu G; Yang Y; He Y
Journal of Human Genetics 2019; 64: 681-687

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