Human Genome Epidemiology Literature Finder
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Records 1 - 10 (of 10 Records) |
| Query Trace: Disease and LTBP2[original query] |
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| Screening of CYP1B1 and LTBP2 genes in Saudi families with primary congenital glaucoma: genotype-phenotype correlation. Molecular vision 2011 17 2911-9. Abu-Amero Khaled K, Osman Essam A, Mousa Ahmed, Wheeler Joshua, Whigham Benjamin, Allingham R Rand, Hauser Michael A, Al-Obeidan Saleh |
| Screening of the LTBP2 gene in a north Indian population with primary congenital glaucoma. Molecular vision 2013 19 . Mohanty K, Tanwar M, Dada R, Dada T |
| Contribution of the latent transforming growth factor-ß binding protein 2 gene to etiology of primary open angle glaucoma and pseudoexfoliation syndrome. Molecular vision 2013 19 333-47. Jelodari-Mamaghani Sahar, Haji-Seyed-Javadi Ramona, Suri Fatemeh, Nilforushan Naveed, Yazdani Shahin, Kamyab Kambiz, Elahi Ela |
| Screening of the LTBP2 gene in 214 Chinese sporadic CYP1B1-negative patients with primary congenital glaucoma. Molecular vision 2016 22 528-35. Chen Xueli, Chen Yuhong, Fan Bao Jian, Xia Mingying, Wang Li, Sun Xinghu |
| Congenital glaucoma and CYP1B1: an old story revisited. Human genetics 2018 3 138 (8-9): 1043-1049. Alsaif Hessa S, Khan Arif O, Patel Nisha, Alkuraya Hisham, Hashem Mais, Abdulwahab Firdous, Ibrahim Niema, Aldahmesh Mohammed A, Alkuraya Fowzan |
| Combination of Panel-based Next-Generation Sequencing and Clinical Findings in Congenital Ectopia Lentis Diagnosed in Chinese Patients. American journal of ophthalmology 2021 Nov . Chen Tian-Hui, Chen Ze-Xu, Zhang Min, Chen Jia-Hui, Deng Michael, Zheng Jia-Lei, Lan Li-Na, Jiang Yong-Xia |
| Exome-based mutation screening in South African children with primary congenital glaucoma. Eye (London, England) 2022 Jan . Carstens Nadia, Goolam Saadiah, Hulley Michaella, Brandenburg Jean-Tristan, Ramsay Michele, Williams Susan Eileen Isabel |
| First Results from the Prospective German Registry for Childhood Glaucoma: Phenotype-Genotype Association. Journal of clinical medicine 2022 1 11 (1): . Stingl Julia V, Diederich Stefan, Diel Heidi, Schuster Alexander K, Wagner Felix M, Chronopoulos Panagiotis, Aghayeva Fidan, Grehn Franz, Winter Jennifer, Schweiger Susann, Hoffmann Esther |
Genome-wide association study reveals novel genetic loci: a new polygenic risk score for mitral valve prolapse.
European heart journal 2022 3 43 (17): 1668-1680. Roselli Carolina, Yu Mengyao, Nauffal Victor, Georges Adrien, Yang Qiong, Love Katie, Weng Lu-Chen, Delling Francesca N, Maurya Svetlana R, Schrölkamp Maren, Tfelt-Hansen Jacob, Hagège Albert, Jeunemaitre Xavier, Debette Stéphanie, Amouyel Philippe, Guan Wyliena, Muehlschlegel Jochen D, Body Simon C, Shah Svati, Samad Zainab, Kyryachenko Sergiy, Haynes Carol, Rienstra Michiel, Le Tourneau Thierry, Probst Vincent, Roussel Ronan, Wijdh-Den Hamer Inez J, Siland Joylene E, Knowlton Kirk U, Jacques Schott Jean, Levine Robert A, Benjamin Emelia J, Vasan Ramachandran S, Horne Benjamin D, Muhlestein Joseph B, Benfari Giovanni, Enriquez-Sarano Maurice, Natale Andrea, Mohanty Sanghamitra, Trivedi Chintan, Shoemaker Moore B, Yoneda Zachary T, Wells Quinn S, Baker Michael T, Farber-Eger Eric, Michelena Hector I, Lundby Alicia, Norris Russell A, Slaugenhaupt Susan A, Dina Christian, Lubitz Steven A, Bouatia-Naji Nabila, Ellinor Patrick T, Milan David |
| The evaluation of targeted exome sequencing of candidate genes in a Han Chinese population with primary open-angle glaucoma. Human molecular genetics 2025 1 . Yiwen Zhou, Youjia Zhang, Qingdan Xu, Xinghuai Sun, Yuhong Ch |
- Page last reviewed:Feb 1, 2024
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