Journal: Ophthalmic genetics - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Journal Ophthalmic genetics

1. "Association of APOE gene polymorphisms with primary open angle glaucoma in Brazilian patients". (2nd January 2021)

Authors:: Occhiutto, Marcelo Luís; de Melo, Mônica Barbosa; Cabral de Vasconcellos, José Paulo; Rodrigues, Thiago Adalton Rosa; Bajano, Flávia Fialho; Costa, Fernando Ferreira; Costa, Vital Paulino
Journal:: Ophthalmic genetics
Issue:: Volume 42:Number 1(2021)
Page Start:: 53
Record Type:: Journal Article
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2. "Eye genetics at the fork in the road" 2017 Franceschetti Lecture, Leeds UK. (3rd May 2020)

Authors:: Mackey, David
Journal:: Ophthalmic genetics
Issue:: Volume 41:Number 3(2020)
Page Start:: 201
Record Type:: Journal Article
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3. "Eye genetics at the fork in the road" 2017 Franceschetti Lecture, Leeds UK. (3rd May 2020)

Authors:: Mackey, David
Journal:: Ophthalmic genetics
Issue:: Volume 41:Number 3(2020)
Page Start:: 201
Record Type:: Journal Article
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4. "Novel p.Tyr284Cys BEST1 genotype–phenotype correlations of Vitelliform Macular Dystrophy in a family with incomplete penetrance". (3rd March 2020)

Authors:: Garza-Garza, Lucas Antonio; León-Cachón, Rafael Baltazar Reyes; Aguirre-Garza, Marcelino; Garza-Leon, Manuel
Journal:: Ophthalmic genetics
Issue:: Volume 41:Number 2(2020)
Page Start:: 183
Record Type:: Journal Article
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5. "Role of polymorphisms of the NLRP3 inflammasome in uveitis". (3rd May 2020)

Authors:: Sarny, Stephanie; Lindner, Ewald; Anticic, Marija; El-Shabrawi, Yosuf
Journal:: Ophthalmic genetics
Issue:: Volume 41:Number 3(2020)
Page Start:: 299
Record Type:: Journal Article
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6. "Role of polymorphisms of the NLRP3 inflammasome in uveitis". (3rd May 2020)

Authors:: Sarny, Stephanie; Lindner, Ewald; Anticic, Marija; El-Shabrawi, Yosuf
Journal:: Ophthalmic genetics
Issue:: Volume 41:Number 3(2020)
Page Start:: 299
Record Type:: Journal Article
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7. 14q22.3 Microdeletion encompassing OTX2 in a five-generation family with microphthalmia, pituitary abnormalities, and intellectual disability. (2nd July 2016)

Authors:: Jones, Gabriela E.; Robertson, Lisa; Warman, Paul; Craft, Emily V.; Cresswell, Lara; Vasudevan, Pradeep C.
Journal:: Ophthalmic genetics
Issue:: Volume 37:Number 3(2016)
Page Start:: 352
Record Type:: Journal Article
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8. 22q11.2 microduplication syndrome and juvenile glaucoma. (4th July 2018)

Authors:: Di Matteo, Federico; Bettin, Paolo; Ferrari, Giulia; Fiori, Marina; Ciampi, Carlo; Manfredini, Emanuela; Rabiolo, Alessandro; Bandello, Francesco
Journal:: Ophthalmic genetics
Issue:: Volume 39:Number 4(2018)
Page Start:: 532
Record Type:: Journal Article
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9. 3D Orbital Reconstruction in a Patient with Microphthalmos and a Large Orbital Cyst—A Case Report. (2nd April 2016)

Authors:: Mourits, D. L.; Wolff, J.; Forouzanfar, T.; Ridwan-Pramana, A.; Moll, A. C.; de Graaf, P.; Remmers, J. S.; Kraal-Biezen, E.; Hartong, D. T.
Journal:: Ophthalmic genetics
Issue:: Volume 37:Number 2(2016)
Page Start:: 233
Record Type:: Journal Article
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10. A 7-year old female with arthrogryposis multiplex congenita, Duane retraction syndrome, and Marcus Gunn phenomenon due to a ZC4H2 gene mutation: a clinical presentation of the Wieacker-Wolff syndrome. (3rd September 2021)

Authors:: Godfrey, Deena; Torres, Alcy; Heidary, Gena; Zahoor, Hovra; Lee, Arthur; Berry, Gerard; Engle, Elizabeth
Journal:: Ophthalmic genetics
Issue:: Volume 42:Number 5(2021)
Page Start:: 612
Record Type:: Journal Article
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