Browsing by Author Alba, Liliana
Showing results 1 to 6 of 6
| Issue Date | Title | Author(s) |
|---|---|---|
| Oct-2004 | Acitretin embryopathy: a case report | Barbero, Pablo ; Lotersztein, Vanesa ; Bronberg, Rubén ; Perez, Miriam ; Alba, Liliana |
| Feb-2006 | Censo de servicios de genética médica en Argentina | Liascovich, Rosa ; Rozental, Sandra ; Barbero, Pablo ; Alba, Liliana ; Ortiz, Zulma |
| Mar-1996 | Microcephaly, characteristic facies, joint abnormalities, and deficient leucocyte chemotaxis: a further case of the syndrome of Say et al | Perandones, Claudia ; Cerretini, Roxana Inés ; Vargas Vera, R M ; Aranda, Eliseo Isaac ; Alba, Liliana ; Pivetta, Omar H. |
| Jun-2008 | Síndrome de insensibilidad completa a los andrógenos : diagnóstico y características clínicas | Solari, Andrea ; Groisman, Boris ; Bidondo, María P. ; Cinca, Constanza ; Alba, Liliana |
| Dec-2016 | Structure-based activity prediction of CYP21A2 stability variants: A survey of available gene variations | Bruque, Carlos D ; Delea, Marisol ; Fernández, Cecilia ; Orza, Juan V ; Taboas, Melisa ; Buzzalino, Noemí ; Espeche, Lucía ; Solari, Andrea ; Luccerini, Verónica ; Alba, Liliana ; Nadra, Alejandro D. ; Dain, Liliana |
| 2011 | Structure-based analysis of five novel disease-causing mutations in 21-hydroxylase-deficient patients | Minutolo, Carolina ; Nadra, Alejandro D. ; Fernández, Cecilia ; Taboas, Melisa ; Buzzalino, Noemí ; Casali, Bárbara ; Belli, Susana ; Charreau, Eduardo H. ; Alba, Liliana ; Dain, Liliana |