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Clinical and Molecular Differences between 4-Year-Old Monozygous Male Twins Mosaic for Normal, Premutation and Fragile X Full Mutation Alleles.
Pandelache, Alison; Baker, Emma K; Aliaga, Solange M; Arpone, Marta; Forbes, Robin; Stark, Zornitza; Francis, David; Godler, David E.
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  • Pandelache A; Victorian Clinical Genetics Services and Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, VIC 3052, Australia. alison.pandelache@vcgs.org.au.
  • Baker EK; Diagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, VIC 3052, Australia. emma.baker@mcri.edu.au.
  • Aliaga SM; Faculty of Medicine, Dentistry and Health Sciences, Department of Paediatrics, University of Melbourne, Parkville, VIC 3052, Australia. emma.baker@mcri.edu.au.
  • Arpone M; Diagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, VIC 3052, Australia. solange.aliagavera@mcri.edu.au.
  • Forbes R; Faculty of Medicine, Dentistry and Health Sciences, Department of Paediatrics, University of Melbourne, Parkville, VIC 3052, Australia. solange.aliagavera@mcri.edu.au.
  • Stark Z; Diagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, VIC 3052, Australia. marta.arpone@mcri.edu.au.
  • Francis D; Faculty of Medicine, Dentistry and Health Sciences, Department of Paediatrics, University of Melbourne, Parkville, VIC 3052, Australia. marta.arpone@mcri.edu.au.
  • Godler DE; Brain and Mind, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, VIC 3052, Australia. marta.arpone@mcri.edu.au.
Genes (Basel) ; 10(4)2019 04 05.
Article en En | MEDLINE | ID: mdl-30959842
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastorno Autístico / Proteína de la Discapacidad Intelectual del Síndrome del Cromosoma X Frágil / Síndrome del Cromosoma X Frágil / Discapacidad Intelectual Límite: Child, preschool / Humans / Male Idioma: En Revista: Genes (Basel) Año: 2019 Tipo del documento: Article País de afiliación: Australia Pais de publicación: Suiza
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastorno Autístico / Proteína de la Discapacidad Intelectual del Síndrome del Cromosoma X Frágil / Síndrome del Cromosoma X Frágil / Discapacidad Intelectual Límite: Child, preschool / Humans / Male Idioma: En Revista: Genes (Basel) Año: 2019 Tipo del documento: Article País de afiliación: Australia Pais de publicación: Suiza