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Ophthalmic Genetics Volume 37, 2016 - Issue 1
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Research Reports

Genotype/Phenotype Correlation in Primary Congenital Glaucoma Patients in the Lebanese Population: A Pilot Study

Christiane Al-HaddadDepartment of Ophthalmology, American University of Beirut Medical Center, Beirut, Lebanon, and
,
Marwan AbdulaalDepartment of Ophthalmology, American University of Beirut Medical Center, Beirut, Lebanon, and
,
Rebecca BadraDepartment of Pathology and Laboratory Medicine, Medical Genetics, American University of Beirut Medical Center, Beirut, Lebanon
,
Anita BarikianDepartment of Ophthalmology, American University of Beirut Medical Center, Beirut, Lebanon, and
,
Bahaa NoureddineDepartment of Ophthalmology, American University of Beirut Medical Center, Beirut, Lebanon, and
&
Chantal FarraDepartment of Pathology and Laboratory Medicine, Medical Genetics, American University of Beirut Medical Center, Beirut, LebanonCorrespondence[email protected]
Pages 31-36 | Received 11 Feb 2014, Accepted 05 May 2014, Published online: 18 Jun 2014

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Nadine J. Makhoul, Zahi Wehbi, Dalia El Hadi, Baha Noureddine, Rose-Mary Boustany & Christiane Al-Haddad. (2023) Whole-exome screening for primary congenital glaucoma in Lebanon. Ophthalmic Genetics 44:3, pages 234-245.
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Sara Jemmeih, Shaza Malik, Sarah Okashah & Hatem Zayed. (2022) Genetic Epidemiology of Primary Congenital Glaucoma in the 22 Arab Countries: A Systematic Review. Ophthalmic Epidemiology 29:1, pages 1-12.
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Claudia Yahalom, Michal Macarov, Galit Lazer-Derbeko, Gheona Altarescu, Tal Imbar, Jordana H. Hyman, Talia Eldar-Geva & Anat Blumenfeld. (2018) Preimplantation genetic diagnosis as a strategy to prevent having a child born with an heritable eye disease. Ophthalmic Genetics 39:4, pages 450-456.
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Articles from other publishers (7)

L. A. Katargina, V. V. Kadyshev, A. A. Sorokin, A. V. Pleskova & R. A. Zinchenko. (2022) Genetic variants of congenital glaucoma. Analysis of the literature and description of the clinical case. Russian Ophthalmological Journal 15:1, pages 105-108.
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Julia V. Stingl, Stefan Diederich, Heidi Diel, Alexander K. Schuster, Felix M. Wagner, Panagiotis Chronopoulos, Fidan Aghayeva, Franz Grehn, Jennifer Winter, Susann Schweiger & Esther M. Hoffmann. (2021) First Results from the Prospective German Registry for Childhood Glaucoma: Phenotype–Genotype Association. Journal of Clinical Medicine 11:1, pages 16.
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Mohamad Dakroub, Diana Khair, Bahaa\' Noureddine & Christiane Al-Haddad. (2021) Pediatric Glaucoma in a University Hospital. Journal of Current Glaucoma Practice 15:1, pages 8-13.
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Viney Gupta, Bindu I. Somarajan, Gagandeep Kaur Walia, Jasbir Kaur, Sunil Kumar, Shikha Gupta, Abadh K. Chaurasia, Dinesh Gupta, Abhinav Kaushik, Aditi Mehta, Vipin Gupta & Arundhati Sharma. (2017) Role of CYP1B1, p.E229K and p.R368H mutations among 120 families with sporadic juvenile onset open-angle glaucoma. Graefe's Archive for Clinical and Experimental Ophthalmology 256:2, pages 355-362.
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Athar Khalil, Christiane Al-Haddad, Hadla Hariri, Kamel Shibbani, Fadi Bitar, Mazen Kurban, Georges Nemer & Mariam Arabi. (2017) A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations. Frontiers in Cardiovascular Medicine 4.
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Mahmoud R. Fassad, Asmaa K. Amin, Heba A. Morsy, Noha M. Issa, Nader H. Bayoumi, Sahar A. El Shafei & Soha F. Kholeif. (2017) CYP1B1 and myocilin gene mutations in Egyptian patients with primary congenital glaucoma. Egyptian Journal of Medical Human Genetics 18:3, pages 219-224.
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Mônica Barbosa de Melo, Anil K. Mandal, Ivan M. Tavares, Mohammed Hasnat Ali, Meha Kabra, José Paulo Cabral de Vasconcellos, Sirisha Senthil, Juliana M. F. Sallum, Inderjeet Kaur, Alberto J. Betinjane, Christiane R. Moura, Jayter S. Paula, Karita A. Costa, Mansoor Sarfarazi, Mauricio Della Paolera, Simone Finzi, Victor E. F. Ferraz, Vital P. Costa, Rubens Belfort & Subhabrata Chakrabarti. (2015) Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and Brazil. PLOS ONE 10:5, pages e0127147.
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