Sfoglia per Autore  

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Mostrati risultati da 1 a 9 di 9
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
Internal validation and improvement of mitochondrial genome sequencing using the Precision ID mtDNA Whole Genome Panel 2021 Faccinetto C.Sabbatini D.Salvoro C.Vazza G. + INTERNATIONAL JOURNAL OF LEGAL MEDICINE - -
Performance of four models for eye color prediction in an Italian population sample 2019 Salvoro, CeciliaFACCINETTO, CHRISTIANPORTO, MARIKAOcchi, GianlucaDE LOS CAMPOS BALTASAR, GUSTAVO AMERICOVazza, Giovanni + FORENSIC SCIENCE INTERNATIONAL: GENETICS - -
Rare Risk Variants Identification by Identity-by-Descent Mapping and Whole-Exome Sequencing Implicates Neuronal Development Pathways in Schizophrenia and Bipolar Disorder 2018 Salvoro, C.Bortoluzzi, S.Coppe, A.Valle, G.Feltrin, E.Mostacciuolo, M. L.Vazza, G. MOLECULAR NEUROBIOLOGY - -
Clinical and genetic characterization of an Italian family with slow-channel syndrome 2018 Angelini, CorradoSalvoro, CeciliaMostacciuolo, Maria LuisaVazza, Giovanni + NEUROLOGICAL SCIENCES - -
Abstracts of the XXIII rd World Congress of Psychiatric Genetics (WCPG): Poster abstracts 2017 Cecilia SalvoroCAMPANELLI, CARLOLivio FinosGiorgio ValleLuisa MostacciuoloStefania BortoluzziGiovanni Vazza EUROPEAN NEUROPSYCHOPHARMACOLOGY - -
Diurnal preference, mood and the response to morning light in relation to polymorphisms in the human clock gene PER3 2017 TURCO, MATTEOBISCONTIN, ALBERTOCACCIN, LAURABANO, MILENACHIAROMANNI, FEDERICASALAMANCA, MARCOSALVORO, CECILIAMAZZOTTA, GABRIELLA MARGHERITADE PITTA', CRISTIANOMONTAGNESE, SARACOSTA, RODOLFO + SCIENTIFIC REPORTS - -
The genetic architecture of schizophrenia and bipolar disorder: identity by descent and exome sequencing in a family-based population sample 2016 Salvoro, Cecilia - - -
Diagnosis of Primary Ciliary Dyskinesia by a Targeted Next-Generation Sequencing Panel: Molecular and Clinical Findings in Italian Patients 2016 BOARETTO, FRANCESCASNIJDERS, DEBORAHSALVORO, CECILIAMOSTACCIUOLO, MARIA LUISABARBATO, ANGELOVAZZA, GIOVANNI + THE JOURNAL OF MOLECULAR DIAGNOSTICS - -
Improving the knowledge of amyotrophic lateral sclerosis genetics: novel SOD1 and FUS variants. 2014 Salvoro CVAZZA, GIOVANNIAngelini CCAGNIN, ANNACHIARAPEGORARO, ELENASORARU', GIANNI + NEUROBIOLOGY OF AGING - -
Mostrati risultati da 1 a 9 di 9
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