For: | Marfany G, Gonzàlez-Duarte R. Clinical applications of high-throughput genetic diagnosis in inherited retinal dystrophies: Present challenges and future directions. World J Med Genet 2015; 5(2): 14-22 [DOI: 10.5496/wjmg.v5.i2.14] |
---|---|
URL: | https://www.wjgnet.com/2220-3184/full/v5/i2/14.htm |
Number | Citing Articles |
1 |
Marta de Castro-Miró, Raul Tonda, Paula Escudero-Ferruz, Rosa Andrés, Andrés Mayor-Lorenzo, Joaquín Castro, Marcela Ciccioli, Daniel A. Hidalgo, Juan José Rodríguez-Ezcurra, Jorge Farrando, Juan J. Pérez-Santonja, Bru Cormand, Gemma Marfany, Roser Gonzàlez-Duarte, Namik Kaya. Novel Candidate Genes and a Wide Spectrum of Structural and Point Mutations Responsible for Inherited Retinal Dystrophies Revealed by Exome Sequencing. PLOS ONE 2016; 11(12): e0168966 doi: 10.1371/journal.pone.0168966
|
2 |
Roser Gonzàlez-Duarte, Marta de Castro-Miró, Miquel Tuson, Valeria Ramírez-Castañeda, Rebeca Valero Gils, Gemma Marfany. Retinal Degenerative Diseases. Advances in Experimental Medicine and Biology 2019; 1185: 215 doi: 10.1007/978-3-030-27378-1_35
|