Your browser doesn't support javascript.
loading
Agreement between parents' and clinical researchers' ratings of behavioral problems in children with fragile X syndrome and chromosome 15 imprinting disorders.
Arpone, Marta; Bretherton, Lesley; Amor, David J; Hearps, Stephen J C; Rogers, Carolyn; Field, Michael J; Hunter, Matthew F; Santa Maria, Lorena; Alliende, Angelica M; Slee, Jennie; Godler, David E; Baker, Emma K.
Afiliação
  • Arpone M; Diagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, VIC, Australia; Department of Paediatrics, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Parkville, VIC, Australia; Brain and Mind, Murdoch Children's Research Insti
  • Bretherton L; Brain and Mind, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, VIC, Australia.
  • Amor DJ; Department of Paediatrics, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Parkville, VIC, Australia; Neurodisability and Rehabilitation, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, VIC, Australia.
  • Hearps SJC; Brain and Mind, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, VIC, Australia; Department of Critical Care, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Parkville, VIC, Australia.
  • Rogers C; Genetics of Learning Disability Service, Hunter Genetics, Waratah, NSW, Australia.
  • Field MJ; Genetics of Learning Disability Service, Hunter Genetics, Waratah, NSW, Australia.
  • Hunter MF; Monash Genetics, Monash Health, Melbourne, VIC, Australia; Department of Paediatrics, Monash University, Melbourne, VIC, Australia.
  • Santa Maria L; Laboratory of Molecular Cytogenetics, Department of Genetics and Metabolic Diseases, Institute of Nutrition and Food Technology (INTA), University of Chile, Santiago, Chile.
  • Alliende AM; Laboratory of Molecular Cytogenetics, Department of Genetics and Metabolic Diseases, Institute of Nutrition and Food Technology (INTA), University of Chile, Santiago, Chile.
  • Slee J; Department of Health, Government of Western Australia, Genetic Services of Western Australia, Perth, Australia.
  • Godler DE; Diagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, VIC, Australia; Department of Paediatrics, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Parkville, VIC, Australia.
  • Baker EK; Diagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, VIC, Australia; Department of Paediatrics, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Parkville, VIC, Australia; School of Psychology and Public Health, La Trobe
Res Dev Disabil ; 131: 104338, 2022 Dec.
Article em En | MEDLINE | ID: mdl-36179574
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Prader-Willi / Comportamento Problema / Síndrome do Cromossomo X Frágil Tipo de estudo: Diagnostic_studies Limite: Child / Female / Humans / Male Idioma: En Revista: Res Dev Disabil Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Prader-Willi / Comportamento Problema / Síndrome do Cromossomo X Frágil Tipo de estudo: Diagnostic_studies Limite: Child / Female / Humans / Male Idioma: En Revista: Res Dev Disabil Ano de publicação: 2022 Tipo de documento: Article