Utilize este identificador para referenciar este registo: http://hdl.handle.net/10400.18/5623
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dc.contributor.authorMarques, Ana Rita-
dc.contributor.authorMartiniano, H.-
dc.contributor.authorSantos, J.X.-
dc.contributor.authorVilela, J.-
dc.contributor.authorAsif, M.-
dc.contributor.authorOliveira, G.-
dc.contributor.authorEnguita, F.J.-
dc.contributor.authorRomão, L.-
dc.contributor.authorVicente, A.M.-
dc.date.accessioned2018-10-22T15:31:59Z-
dc.date.available2018-10-22T15:31:59Z-
dc.date.issued2018-06-
dc.identifier.urihttp://hdl.handle.net/10400.18/5623-
dc.descriptionA.R.Marques is recipiente of a fellowship from BioSys PhD programme (Ref PD/BD/113773/2015 from FCT (Portugal). Patients and parents were genotyped in the context of the Autism Genome Project (AGP), funded by NIMH, HRB, MRC, Autism Speaks, Hilibrand Foundation, Genome Canada, OGI, CIHR, and the Simons Simplex Collection (SSC), a core project of the Simons Foundation Autism Research Initiative (SFARI).pt_PT
dc.descriptionPrémio melhor posterpt_PT
dc.description.abstractIntroduction: Autism Spectrum Disorder (ASD) is a neurodevelopmental disorder: Characterized by deficits in social communication/interaction and by unusual repetitive and restricted behaviors and interests; Median estimated prevalence worldwide is 17/10000; Male to female ratio: ~4:1; Comorbidities: intellectual disability, anxiety, epilepsy, (…).pt_PT
dc.description.sponsorshipA.R.Marques is recipient of a fellowship from BioSys PhD programme (Ref PD/BD/113773/2015 from FCT (Portugal). Patients and parents were genotyped in the context of the Autism Genome Project (AGP), funded by NIMH, HRB, MRC, Autism Speaks, Hilibrand Foundation, Genome Canada, OGI, CIHR, and the Simons Simplex Collection (SSC), a core project of the Simons Foundation Autism Research Initiative (SFARI).pt_PT
dc.language.isoengpt_PT
dc.publisherInstituto Nacional de Saúde Doutor Ricardo Jorge, IPpt_PT
dc.rightsembargoedAccesspt_PT
dc.subjectAutism Spectrum Disorderpt_PT
dc.subjectPerturbações do Desenvolvimento Infantil e Saúde Mentalpt_PT
dc.subjectmiRNA Genept_PT
dc.subjectlncRNA Genept_PT
dc.titlemiRNA and lncRNA gene variants in Autism Spectrum Disorderpt_PT
dc.typeconferenceObjectpt_PT
dc.description.versionN/Apt_PT
degois.publication.locationMilão, itáliapt_PT
degois.publication.title52nd European Society of Human Genetics (ESHG), june 16-19 2018pt_PT
Aparece nas colecções:DPSPDNT - Posters/abstracts em congressos internacionais



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