Search Results - Katzaki, E.

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  1. 1
    The XLMR gene ACSL4 plays a role in dendritic spine architecture

    The XLMR gene ACSL4 plays a role in dendritic spine architecture by Meloni, I, Parri, V, De Filippis, R, Ariani, F, Artuso, R, Bruttini, M, Katzaki, E, Longo, I, Mari, F, Bellan, C, Dotti, C.G, Renieri, A

    Published in Neuroscience
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  2. 2
    Xq28 duplications including MECP2 in five females: Expanding the phenotype to severe mental retardation

    Xq28 duplications including MECP2 in five females: Expanding the phenotype to severe mental retardation by Bijlsma, E.K, Collins, A, Papa, F.T, Tejada, M.I, Wheeler, P, Peeters, E.A.J, Gijsbers, A.C.J, van de Kamp, J.M, Kriek, M, Losekoot, M, Broekma, A.J, Crolla, J.A, Pollazzon, M, Mucciolo, M, Katzaki, E, Disciglio, V, Ferreri, M.I, Marozza, A, Mencarelli, M.A, Castagnini, C, Dosa, L, Ariani, F, Mari, F, Canitano, R, Hayek, G, Botella, M.P, Gener, B, Mínguez, M, Renieri, A, Ruivenkamp, C.A.L

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  3. 3
    A 9.3 Mb microdeletion of 3q27.3q29 associated with psychomotor and growth delay, tricuspid valve dysplasia and bifid thumb

    A 9.3 Mb microdeletion of 3q27.3q29 associated with psychomotor and growth delay, tricuspid valve dysplasia and bifid thumb by Pollazzon, M, Grosso, S, Papa, F.T, Katzaki, E, Marozza, A, Mencarelli, M.A, Uliana, V, Balestri, P, Mari, F, Renieri, A

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  4. 4
    A 9.3Mb microdeletion of 3q27.3q29 associated with psychomotor and growth delay, tricuspid valve dysplasia and bifid thumb

    A 9.3Mb microdeletion of 3q27.3q29 associated with psychomotor and growth delay, tricuspid valve dysplasia and bifid thumb by Pollazzon, M., Grosso, S., Papa, F.T., Katzaki, E., Marozza, A., Mencarelli, M.A., Uliana, V., Balestri, P., Mari, F., Renieri, A.

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  5. 5
    A 9.3 Mb microdeletion of 3q27.3q29 associated with psychomotor and growth delay, tricuspid valve dysplasia and bifid thumb: Emerging Microdeletion and Microduplication Syndromes

    A 9.3 Mb microdeletion of 3q27.3q29 associated with psychomotor and growth delay, tricuspid valve dysplasia and bifid thumb: Emerging Microdeletion and Microduplication Syndromes by POLLAZZON, M, GROSSO, S, PAPA, F. T, KATZAKI, E, MAROZZA, A, MENCARELLI, M. A, ULIANA, V, BALESTRI, P, MARI, F, RENIERI, A

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  6. 6
    Array comparative genomic hybridization in retinoma and retinoblastoma tissues

    Array comparative genomic hybridization in retinoma and retinoblastoma tissues by Sampieri, Katia, Amenduni, Mariangela, Papa, Filomena Tiziana, Katzaki, Eleni, Mencarelli, Maria Antonietta, Marozza, Annabella, Epistolato, Maria Carmela, Toti, Paolo, Lazzi, Stefano, Bruttini, Mirella, De Filippis, Roberta, De Francesco, Sonia, Longo, Ilaria, Meloni, Ilaria, Mari, Francesca, Acquaviva, Antonio, Hadjistilianou, Theodora, Renieri, Alessandra, Ariani, Francesca

    Published in Cancer science
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  7. 7
    High frequency of COH1 intragenic deletions and duplications detected by MLPA in patients with Cohen syndrome

    High frequency of COH1 intragenic deletions and duplications detected by MLPA in patients with Cohen syndrome by Parri, Veronica, Katzaki, Eleni, Uliana, Vera, Scionti, Francesca, Tita, Rossella, Artuso, Rosangela, Longo, Ilaria, Boschloo, Renske, Vijzelaar, Raymon, Selicorni, Angelo, Brancati, Francesco, Dallapiccola, Bruno, Zelante, Leopoldo, Hamel, Christian P, Sarda, Pierre, Lalani, Seema R, Grasso, Rita, Buoni, Sabrina, Hayek, Joussef, Servais, Laurent, de Vries, Bert B A, Georgoudi, Nelly, Nakou, Sheena, Petersen, Michael B, Mari, Francesca, Renieri, Alessandra, Ariani, Francesca

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