The Genetic Causes of Nonsyndromic Congenital Retinal Detachment: A Genetic and Phenotypic Study of Pakistani Families

por Keser, Vafa, Khan, Ayesha, Siddiqui, Sorath, Lopez, Irma, Ren, Huanan, Qamar, Raheel, Nadaf, Javad, Majewski, Jacek, Chen, Rui, Koenekoop, Robert K.
Publicado 2017

Snap29 mutant mice recapitulate neurological and ophthalmological abnormalities associated with 22q11 and CEDNIK syndrome

por Keser, Vafa, Lachance, Jean-François Boisclair, Alam, Sabrina Shameen, Lim, Youngshin, Scarlata, Eleonora, Kaur, Apinder, Zhang, Tian Fang, Lv, Shasha, Lachapelle, Pierre, O’Flaherty, Cristian, Golden, Jeffrey A., Jerome-Majewska, Loydie A.
Publicado 2019