A cohort study of neurodevelopmental disorders and/or congenital anomalies using high resolution chromosomal microarrays in southern Brazil highlighting the significance of ASD.

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作者： Tiago Fernando,Chaves ^[1] ; Maristela,Ocampos ^[2] ; Ingrid Tremel,Barbato ^[3] ; Louise Lapagesse,de Camargo Pinto ^[4] ; Gisele Rozone,de Luca ^[5] ; Jorge Humberto,Barbato Filho ^[6] ; Priscila,Bernardi ^[6] ; Yara,Costa Netto Muniz ^[5] ; Angelica,Francesca Maris ^[7]

作者单位： Laboratório de Polimorfismos Genéticos (LAPOGE), Universidade Federal de Santa Catarina, Florianópolis, SC, Brazil. tiagochavo@msn.com. ^[1] Universidade Federal de Santa Catarina, Florianópolis, SC, Brazil. tiagochavo@msn.com. ^[2] Laboratory Neurogene (former), Florianopolis, SC, Brazil. ^[3] Mercolab Diagnóstica (actual), Florianopolis, SC, Brazil. ^[4] Laboratory Neurogene, Florianópolis, SC, Brazil. ^[5] Children's Hospital Joana de Gusmão, Florianópolis, SC, Brazil. ^[6] University Hospital Professor Polydoro Ernani de São Thiago, Florianópolis, SC, Brazil. ^[7] Laboratório de Polimorfismos Genéticos (LAPOGE), Universidade Federal de Santa Catarina, Florianópolis, SC, Brazil. ^[8] Universidade Federal de Santa Catarina, Florianópolis, SC, Brazil. afmaris@gmail.com. ^[9] Children's Hospital Joana de Gusmão, Florianópolis, SC, Brazil. afmaris@gmail.com. ^[10]

关键词 Autism Brazil Chromosomal microarrays Congenital anomalies Copy number variations LCSH Neurodevelopmental disorders