Search Results - Oliveri, Jaen

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  1. 1
    Spastic ataxia with eye-of-the-tiger-like sign in 4 siblings due to novel compound heterozygous AFG3L2 mutation

    Spastic ataxia with eye-of-the-tiger-like sign in 4 siblings due to novel compound heterozygous AFG3L2 mutation by Calandra, Cristian R., Buda, Guadalupe, Vishnopolska, Sebastian A., Oliveri, Jaen, Olivieri, Federico A., Pérez Millán, María I., Biagioli, German, Miquelini, Luis A., Pellene, Alejandro L., Marti, Marcelo A.

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  2. 2
    Genetic Analysis Algorithm for the Study of Patients with Multiple Congenital Anomalies and Isolated Congenital Heart Disease

    Genetic Analysis Algorithm for the Study of Patients with Multiple Congenital Anomalies and Isolated Congenital Heart Disease by Delea, Marisol, Massara, Lucia S, Espeche, Lucia D, Bidondo, María Paz, Barbero, Pablo, Oliveri, Jaen, Brun, Paloma, Fabro, Mónica, Galain, Micaela, Fernández, Cecilia S, Taboas, Melisa, Bruque, Carlos D, Kolomenski, Jorge E, Izquierdo, Agustín, Berenstein, Ariel, Cosentino, Viviana, Martinoli, Celeste, Vilas, Mariana, Rittler, Mónica, Mendez, Rodrigo, Furforo, Lilian, Liascovich, Rosa, Groisman, Boris, Rozental, Sandra, Dain, Liliana, On Behalf Of The Pid Acm-Cc Group

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  3. 3
    Gordon Holmes Syndrome Caused by RNF216 Novel Mutation in 2 Argentinean Siblings

    Gordon Holmes Syndrome Caused by RNF216 Novel Mutation in 2 Argentinean Siblings by Calandra, Cristian R., Mocarbel, Yamile, Vishnopolska, Sebastian A., Toneguzzo, Vanessa, Oliveri, Jaen, Cazado, Enrique Carlos, Biagioli, German, Turjanksi, Adrián G., Marti, Marcelo

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  4. 4
    Acephaly: Further Evidence for Disruption but Not for Amniotic Bands

    Acephaly: Further Evidence for Disruption but Not for Amniotic Bands by Mazzitelli, Nancy, Vauthay, Liliana, Oliveri, Jaen, Maccarone, Belen, Rittler, Monica

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  5. 5
    Genetic Imbalances in Argentinean Patients with Congenital Conotruncal Heart Defects

    Genetic Imbalances in Argentinean Patients with Congenital Conotruncal Heart Defects by Delea, Marisol, Espeche, Lucía D, Bruque, Carlos D, Bidondo, María Paz, Massara, Lucía S, Oliveri, Jaen, Brun, Paloma, Cosentino, Viviana R, Martinoli, Celeste, Tolaba, Norma, Picon, Claudina, Ponce Zaldua, María Eugenia, Ávila, Silvia, Gutnisky, Viviana, Perez, Myriam, Furforo, Lilian, Buzzalino, Noemí D, Liascovich, Rosa, Groisman, Boris, Rittler, Mónica, Rozental, Sandra, Barbero, Pablo, Dain, Liliana

    Published in Genes
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  6. 6
    Spastic ataxia with eye-of-the-tiger-like sign in 4 siblings due to novel compound heterozygous AFG3L2 mutation

    Spastic ataxia with eye-of-the-tiger-like sign in 4 siblings due to novel compound heterozygous AFG3L2 mutation by Calandra, Cristian R, Buda, Guadalupe, Vishnopolska, Sebastian A, Oliveri, Jaen, Olivieri, Federico A, Pérez Millán, María I, Biagioli, German, Miquelini, Luis A, Pellene, Alejandro L, Marti, Marcelo A

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  7. 7
    Gordon Holmes Syndrome Caused by RNF216 Novel Mutation in 2 Argentinean Siblings

    Gordon Holmes Syndrome Caused by RNF216 Novel Mutation in 2 Argentinean Siblings by Calandra, Cristian R, Mocarbel, Yamile, Vishnopolska, Sebastian A, Toneguzzo, Vanessa, Oliveri, Jaen, Cazado, Enrique Carlos, Biagioli, German, Turjanksi, Adrián G, Marti, Marcelo

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