يعرض 1 - 3 نتائج من 3 نتيجة بحث عن '"Romaniello, Romina"', وقت الاستعلام: 0.72s تنقيح النتائج
  1. 1
    دورية أكاديمية
    Delineation and diagnostic criteria of Oral-Facial-Digital Syndrome type VI

    المؤلفون: Poretti, Andrea, Vitiello, Giuseppina, Hennekam, Raoul C M, Arrigoni, Filippo, Bertini, Enrico, Borgatti, Renato, Brancati, Francesco, D'Arrigo, Stefano, Faravelli, Francesca, Giordano, Lucio, Huisman, Thierry A G M, Iannicelli, Miriam, Kluger, Gerhard, Kyllerman, Marten, Landgren, Magnus, Lees, Melissa M, Pinelli, Lorenzo, Romaniello, Romina, Scheer, Ianina, Schwarz, Christoph E, Spiegel, Ronen, Tibussek, Daniel, Valente, Enza Maria, Boltshauser, Eugen

    المصدر: Poretti, Andrea; Vitiello, Giuseppina; Hennekam, Raoul C M; Arrigoni, Filippo; Bertini, Enrico; Borgatti, Renato; Brancati, Francesco; D'Arrigo, Stefano; Faravelli, Francesca; Giordano, Lucio; Huisman, Thierry A G M; Iannicelli, Miriam; Kluger, Gerhard; Kyllerman, Marten; Landgren, Magnus; Lees, Melissa M; Pinelli, Lorenzo; Romaniello, Romina; Scheer, Ianina; Schwarz, Christoph E; Spiegel, Ronen; Tibussek, Daniel; Valente, Enza Maria; Boltshauser, Eugen (2012). Delineation and diagnostic criteria of Oral-Facial-Digital Syndrome type VI. Orphanet Journal of Rare Diseases, 7:4.

    مصطلحات موضوعية: Medical Clinic, 610 Medicine & health

    وصف الملف: application/pdf

    العلاقة: https://www.zora.uzh.ch/id/eprint/73303/1/1750-1172-7-4.pdfTest; info:pmid/22236771; urn:issn:1750-1172

    الإتاحة: https://doi.org/10.5167/uzh-7330310.1186/1750-1172-7-4Test
    https://www.zora.uzh.ch/id/eprint/73303Test/
    https://www.zora.uzh.ch/id/eprint/73303/1/1750-1172-7-4.pdfTest

    View record in BASE النص الكامل

    أضف إلى المفضلة
  2. 2
    دورية أكاديمية
    Targeted next-generation sequencing identifies the disruption of the SHANK3 and RYR2 genes in a patient carrying a de novo t(1;22)(q43;q13.3) associated with signs of Phelan-McDermid syndrome.

    المؤلفون: Bonaglia, Maria Clara, Bertuzzo, Sara, Ciaschini, Anna Maria, Discepoli, Giancarlo, Castiglia, Lucia, Romaniello, Romina, Zuffardi, Orsetta, Fichera, Marco

    المصدر: Molecular Cytogenetics (17558166); 6/11/2020, Vol. 13 Issue 1, p1-8, 8p

    مصطلحات موضوعية: NUCLEOTIDE sequencing, GENE mapping, CEREBRAL cortex, GENE fusion, HUMAN abnormalities, CHROMOSOMAL translocation

    النص الكامل

    أضف إلى المفضلة
  3. 3
    دورية أكاديمية
    Virtual Reality Social Prediction Improvement and Rehabilitation Intensive Training (VR-SPIRIT) for paediatric patients with congenital cerebellar diseases: study protocol of a randomised controlled trial.

    المؤلفون: Butti, Niccolò, Biffi, Emilia, Genova, Chiara, Romaniello, Romina, Redaelli, Davide Felice, Reni, Gianluigi, Borgatti, Renato, Urgesi, Cosimo

    المصدر: Trials; 1/14/2020, Vol. 21 Issue 1, p1-12, 12p, 1 Color Photograph, 3 Charts

    مصطلحات موضوعية: CONGENITAL disorders, VIRTUAL reality, PROPHECY, SOCIAL reality, REHABILITATION, SOCIAL perception, SOCIAL skills

    النص الكامل

    أضف إلى المفضلة
أدوات البحث: أحصل على تغذية RSS — أرسل هذا البحث بالبريد الإلكتروني — حفظ البحث