Treffer 1 - 4 von 4 für Suche 'Ventruto, Maria Luisa', Suchdauer: 0,42s Treffer weiter einschränken
  1. 1
    A t(2;8) Balanced Translocation with Breakpoints Near the Human HOXD Complex Causes Mesomelic Dysplasia and Vertebral Defects

    A t(2;8) Balanced Translocation with Breakpoints Near the Human HOXD Complex Causes Mesomelic Dysplasia and Vertebral Defects von Spitz, François, Montavon, Thomas, Monso-Hinard, Christine, Morris, Michael, Ventruto, Maria-Luisa, Antonarakis, Stylianos, Ventruto, Valerio, Duboule, Denis

    Veröffentlicht in Genomics (San Diego, Calif.)

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  2. 2
    Duplication of Yq- and proximal Yp-arms with deletion of almost all PAR1 (including SHOX) in a young man with non-obstructive azoospermia, short stature and skeletal defects

    Duplication of Yq- and proximal Yp-arms with deletion of almost all PAR1 (including SHOX) in a young man with non-obstructive azoospermia, short stature and skeletal defects von Cancemi, Dino, Iannuzzi, Alessandra, Perucatti, Angela, Montano, Luigi, Capozzi, Oronzo, Spampanato, Carmine, Ventruto, Maria Luisa, Urciuoli, Maria, Iannuzzi, Leopoldo, Ventruto, Valerio

    Veröffentlicht in Journal of applied genetics

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  3. 3
    Malattie genetiche nella medicina prenatale

    Malattie genetiche nella medicina prenatale von Borrelli, Antonio L, Ventruto, Valerio, Arduini, Domenico, Cardone, Antonio

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  4. 4
    Ocular signs associated with a rhodopsin mutation (Cys-167→Arg) in a family with autosomal dominant retinitis pigmentosa

    Ocular signs associated with a rhodopsin mutation (Cys-167→Arg) in a family with autosomal dominant retinitis pigmentosa von SIMONELLI, FRANCESCA, RINALDI, MARIO, NESTI, ANNA, TESTA, FRANCESCO, RINALDI, ERNESTO, CICCODICOLA, ALFREDO, FLAGIELLO, LUISA, MIANO, MARIA GIUSEPPINA, VENTRUTO, VALERIO, D’URSO, MICHELE


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