Canlyniadau Chwilio - Arianna Vino

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  1. 1
    A de novo FOXP1 variant in a patient with autism, intellectual disability and severe speech and language impairment

    A de novo FOXP1 variant in a patient with autism, intellectual disability and severe speech and language impairment gan Reymundo Lozano, Arianna Vino, Cristina Lozano, Simon E. Fisher, Pelagia Deriziotis

    Cyhoeddwyd 2015
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  2. 2
    Rare variants in axonogenesis genes connect three families with sound–color synesthesia

    Rare variants in axonogenesis genes connect three families with sound–color synesthesia gan Amanda K. Tilot, Katerina S. Kucera, Arianna Vino, Julian E. Asher, Simon Baron‐Cohen, Simon E. Fisher

    Cyhoeddwyd 2018
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  3. 3
    Prevalence of <i>Borrelia Burgdorferi</i> Infection in a Series of 98 Primary Cutaneous Lymphomas

    Prevalence of <i>Borrelia Burgdorferi</i> Infection in a Series of 98 Primary Cutaneous Lymphomas gan Maurilio Ponzoni, Andrés J.M. Ferreri, Silvia Mappa, Elisa Pasini, Silvia Govi, Fabio Facchetti, Daniele Fanoni, Alessandra Tucci, Arianna Vino, Claudio Doglioni, Emilio Berti, Riccardo Dolcetti

    Cyhoeddwyd 2011
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  4. 4
    Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disorders

    Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disorders gan Sara B. Estruch, Sarah A. Graham, Martí Quevedo, Arianna Vino, Dick H. W. Dekkers, Pelagia Derizioti, Elliot Sollis, Jeroen Demmers, Raymond A. Poot, Simon E. Fisher

    Cyhoeddwyd 2018
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  5. 5
    Identification and functional characterization of<i>de novo FOXP1</i>variants provides novel insights into the etiology of neurodevelopmental disorder

    Identification and functional characterization of<i>de novo FOXP1</i>variants provides novel insights into the etiology of neurodevelopmental disorder gan Elliot Sollis, Sarah A. Graham, Arianna Vino, Henning Froehlich, Maaike Vreeburg, D. Dimitropoulou, Christian Gilissen, Rolph Pfundt, Gudrun Rappold, Han G. Brunner, Pelagia Derizioti, Simon E. Fisher

    Cyhoeddwyd 2015
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  6. 6
    A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development

    A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development gan Else Eising, Amaia Carrión-Castillo, Arianna Vino, Edythe A. Strand, Kathy J. Jakielski, Thomas Scerri, Michael S. Hildebrand, Richard Webster, Alan Ma, Bernard Mazoyer, Clyde Francks, Melanie Bahlo, Ingrid E. Scheffer, Angela Morgan, Lawrence D. Shriberg, Simon E. Fisher

    Cyhoeddwyd 2018
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    Ychwanegu at ffefrynnau
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  7. 7
    Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations

    Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations gan Dervla M. Connaughton, Rufeng Dai, Danielle Owen, Jonathan Marquez, Nina Mann, Adda L. Graham-Paquin, Makiko Nakayama, Étienne Coyaud, Estelle Laurent, Jonathan St‐Germain, Lot Snijders Blok, Arianna Vino, Verena Klämbt, Konstantin Deutsch, Chen-Han Wilfred Wu, Caroline M. Kolvenbach, Franziska Kause, Isabel Ottlewski, Ronen Schneider, Thomas M. Kitzler, Amar J. Majmundar, Florian Buerger, Ana C. Onuchic-Whitford, Youying Mao, Amy Kolb, Daanya Salmanullah, Evan Chen, Amelie T. van der Ven, Jia Rao, Hadas Ityel, Steve Seltzsam, Johanna M. Rieke, Jing Chen, Asaf Vivante, Daw‐Yang Hwang, Stefan Kohl, Gabriel C. Dworschak, Tobias Hermle, Mariëlle Alders, Tobias Bartolomaeus, Stuart B. Bauer, Michelle A. Baum, Eva H. Brilstra, Thomas D. Challman, Jacob Zyskind, Carrie E. Costin, Katrina M. Dipple, Floor A.M. Duijkers, Marcia Ferguson, David Fitzpatrick, Roger Fick, Ian Glass, Peter J. Hulick, Antonie D. Kline, Ilona Krey, Selvin Kumar, Lu W, Elysa J. Marco, Ingrid M. Wentzensen, Heather C. Mefford, Konrad Platzer, Inna Povolotskaya, Juliann M. Savatt, Н. В. Щербакова, Prabha Senguttuvan, Audrey Squire, Deborah R. Stein, Isabelle Thiffault, V. Yu. Voinova, Michael J. Somers, Michael A. Ferguson, Avram Z. Traum, Ghaleb H. Daouk, Ankana Daga, Nancy Rodig, Paulien A. Terhal, Ellen van Binsbergen, Loai Eid, Velibor Tasić, Hila Milo Rasouly, Tze Y. Lim, Dina Ahram, Ali G. Gharavi, Heiko Reutter, Heidi L. Rehm, Daniel G. MacArthur, Monkol Lek, Kristen M. Laricchia, Richard P. Lifton, Hong Xu, Shrikant Mane, Simone Sanna‐Cherchi, Andrew D. Sharrocks, Brian Raught, Simon E. Fisher, Maxime Bouchard, Mustafa K. Khokha, Shirlee Shril, Friedhelm Hildebrandt

    Cyhoeddwyd 2020
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