Search Results - Orera-Clemente, María

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  1. 1
    Clinical report of Bosma arhinia microphthalmia syndrome with a new variant on SMCHD1 gene. A case report

    Clinical report of Bosma arhinia microphthalmia syndrome with a new variant on SMCHD1 gene. A case report by Atencia Goñi, José, Orera Clemente, María, Del Valle Diéguez, Mariano José, González Fernández, Laura, González Albarrán, Olga

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    Prenatal diagnosis of Bardet–Biedl syndrome in a case of hyperechogenic kidneys: Clinical use of DNA sequencing

    Prenatal diagnosis of Bardet–Biedl syndrome in a case of hyperechogenic kidneys: Clinical use of DNA sequencing by Garcia‐Tizon Larroca, Santiago, Blagoeva Atanasova, Vangeliya, Orera Clemente, Maria, Aluja Mendez, Anna, Ortega Abad, Virginia, Perez Fernandez‐Pacheco, Ricardo, De León Luis, Juan, Gamez Alderete, Francisco

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    Recommendations regarding the genetic and immunological study of reproductive dysfunction

    Recommendations regarding the genetic and immunological study of reproductive dysfunction by Alonso-Cerezo, María Concepción, Calero Ruiz, Mercedes, Chantada-Abal, Venancio, de la Fuente-Hernández, Luis Alfonso, García-Cobaleda, Inmaculada, García-Ochoa, Carlos, García-Sagredo, José Miguel, Nuñez, Rocío, Oliva, Rafael, Orera-Clemente, María, Pintado-Vera, David, Sanchez-Ramon, Silvia

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  4. 4
    Prenatal diagnosis of Bardet-Biedl syndrome in a case of hyperechogenic kidneys: Clinical use of DNA sequencing

    Prenatal diagnosis of Bardet-Biedl syndrome in a case of hyperechogenic kidneys: Clinical use of DNA sequencing by Garcia-Tizon Larroca, Santiago, Blagoeva Atanasova, Vangeliya, Orera Clemente, Maria, Aluja Mendez, Anna, Ortega Abad, Virginia, Perez Fernandez-Pacheco, Ricardo, De León Luis, Juan, Gamez Alderete, Francisco

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