Αποτελέσματα αναζήτησης - Villanueva, Adda
- Εμφανίζονται 1 - 4 Αποτελέσματα από 4
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Whole Exome Sequencing of a Dominant Retinitis Pigmentosa Family Identifies a Novel Deletion in PRPF31 από Villanueva, Adda, Willer, Jason R., Bryois, Julien, Dermitzakis, Emmanouil T., Katsanis, Nicholas, Davis, Erica E.
Έκδοση 2014Κείμενο -
2
Utility of In Vitro Mutagenesis of RPE65 Protein for Verification of Mutational Pathogenicity Before Gene Therapy από Yang, Unikora, Gentleman, Susan, Gai, Xiaowu, Gorin, Michael B., Borchert, Mark S., Lee, Thomas C., Villanueva, Adda, Koenekoop, Robert, Maguire, Albert M., Bennett, Jean, Redmond, T. Michael, Nagiel, Aaron
Έκδοση 2019Κείμενο -
3
Identification of the genetic determinants responsible for retinal degeneration in families of Mexican descent από Villanueva, Adda, Biswas, Pooja, Kishaba, Kameron, Suk, John, Tadimeti, Keerti, Raghavendra, P.B, Nadeau, Karine, Lamontagne, Bruno, Busque, Lambert, Geoffroy, Steve, Mongrain, Ian, Asselin, Géraldine, Provost, Sylvie, Dubé, Marie-Pierre, Nudleman, Eric, Ayyagari, Radha
Έκδοση 2017Κείμενο -
4
Deciphering the genetic architecture and ethnographic distribution of IRD in three ethnic populations by whole genome sequence analysis από Biswas, Pooja, Villanueva, Adda L., Soto-Hermida, Angel, Duncan, Jacque L., Matsui, Hiroko, Borooah, Shyamanga, Kurmanov, Berzhan, Richard, Gabriele, Khan, Shahid Y., Branham, Kari, Huang, Bonnie, Suk, John, Bakall, Benjamin, Goldberg, Jeffrey L., Gabriel, Luis, Khan, Naheed W., Raghavendra, Pongali B., Zhou, Jason, Devalaraja, Sindhu, Huynh, Andrew, Alapati, Akhila, Zawaydeh, Qais, Weleber, Richard G., Heckenlively, John R., Hejtmancik, J. Fielding, Riazuddin, Sheikh, Sieving, Paul A., Riazuddin, S. Amer, Frazer, Kelly A., Ayyagari, Radha
Έκδοση 2021Κείμενο