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Tissue mosaicism, FMR1 expression and intellectual functioning in males with fragile X syndrome.

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Title: Tissue mosaicism, FMR1 expression and intellectual functioning in males with fragile X syndrome.
Authors: Baker EK; Diagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Victoria, Australia.; Department of Paediatrics, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Parkville, Victoria, Australia.; School of Psychology and Public Health, La Trobe University, Bundoora, Victoria, Australia., Arpone M; Diagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Victoria, Australia.; Department of Paediatrics, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Parkville, Victoria, Australia.; Brain and Mind, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia., Bui M; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Melbourne, Victoria, Australia., Kraan CM; Diagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Victoria, Australia.; Department of Paediatrics, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Parkville, Victoria, Australia., Ling L; Diagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Victoria, Australia., Francis D; Victorian Clinical Genetics Services and Murdoch Children's Research Institute, The Royal Children's Hospital, Melbourne, Victoria, Australia., Hunter MF; Monash Genetics, Monash Health, Clayton, Victoria, Australia.; Department of Paediatrics, Monash University, Clayton, Victoria, Australia., Rogers C; Genetics of Learning Disability Service, Hunter Genetics, Waratah, New South Wales, Australia., Field MJ; Genetics of Learning Disability Service, Hunter Genetics, Waratah, New South Wales, Australia., Santa María L; Molecular and Cytogenetics Laboratory, INTA University of Chile, Santiago, Chile., Faundes V; Molecular and Cytogenetics Laboratory, INTA University of Chile, Santiago, Chile., Curotto B; Molecular and Cytogenetics Laboratory, INTA University of Chile, Santiago, Chile., Morales P; Molecular and Cytogenetics Laboratory, INTA University of Chile, Santiago, Chile., Trigo C; Molecular and Cytogenetics Laboratory, INTA University of Chile, Santiago, Chile., Salas I; Molecular and Cytogenetics Laboratory, INTA University of Chile, Santiago, Chile., Alliende AM; Molecular and Cytogenetics Laboratory, INTA University of Chile, Santiago, Chile., Amor DJ; Department of Paediatrics, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Parkville, Victoria, Australia.; Neurodisability and Rehabilitation, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Victoria, Australia., Godler DE; Diagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Victoria, Australia.; Department of Paediatrics, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Parkville, Victoria, Australia.
Source: American journal of medical genetics. Part A [Am J Med Genet A] 2023 Feb; Vol. 191 (2), pp. 357-369. Date of Electronic Publication: 2022 Nov 08.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Tissue mosaicism, FMR1 expression and intellectual functioning in males with fragile X syndrome.
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  Data: <searchLink fieldCode="AU" term="%22Baker+EK%22">Baker EK</searchLink>; Diagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Victoria, Australia.; Department of Paediatrics, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Parkville, Victoria, Australia.; School of Psychology and Public Health, La Trobe University, Bundoora, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22Arpone+M%22">Arpone M</searchLink>; Diagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Victoria, Australia.; Department of Paediatrics, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Parkville, Victoria, Australia.; Brain and Mind, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22Bui+M%22">Bui M</searchLink>; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Melbourne, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22Kraan+CM%22">Kraan CM</searchLink>; Diagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Victoria, Australia.; Department of Paediatrics, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Parkville, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22Ling+L%22">Ling L</searchLink>; Diagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22Francis+D%22">Francis D</searchLink>; Victorian Clinical Genetics Services and Murdoch Children's Research Institute, The Royal Children's Hospital, Melbourne, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22Hunter+MF%22">Hunter MF</searchLink>; Monash Genetics, Monash Health, Clayton, Victoria, Australia.; Department of Paediatrics, Monash University, Clayton, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22Rogers+C%22">Rogers C</searchLink>; Genetics of Learning Disability Service, Hunter Genetics, Waratah, New South Wales, Australia.<br /><searchLink fieldCode="AU" term="%22Field+MJ%22">Field MJ</searchLink>; Genetics of Learning Disability Service, Hunter Genetics, Waratah, New South Wales, Australia.<br /><searchLink fieldCode="AU" term="%22Santa+María+L%22">Santa María L</searchLink>; Molecular and Cytogenetics Laboratory, INTA University of Chile, Santiago, Chile.<br /><searchLink fieldCode="AU" term="%22Faundes+V%22">Faundes V</searchLink>; Molecular and Cytogenetics Laboratory, INTA University of Chile, Santiago, Chile.<br /><searchLink fieldCode="AU" term="%22Curotto+B%22">Curotto B</searchLink>; Molecular and Cytogenetics Laboratory, INTA University of Chile, Santiago, Chile.<br /><searchLink fieldCode="AU" term="%22Morales+P%22">Morales P</searchLink>; Molecular and Cytogenetics Laboratory, INTA University of Chile, Santiago, Chile.<br /><searchLink fieldCode="AU" term="%22Trigo+C%22">Trigo C</searchLink>; Molecular and Cytogenetics Laboratory, INTA University of Chile, Santiago, Chile.<br /><searchLink fieldCode="AU" term="%22Salas+I%22">Salas I</searchLink>; Molecular and Cytogenetics Laboratory, INTA University of Chile, Santiago, Chile.<br /><searchLink fieldCode="AU" term="%22Alliende+AM%22">Alliende AM</searchLink>; Molecular and Cytogenetics Laboratory, INTA University of Chile, Santiago, Chile.<br /><searchLink fieldCode="AU" term="%22Amor+DJ%22">Amor DJ</searchLink>; Department of Paediatrics, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Parkville, Victoria, Australia.; Neurodisability and Rehabilitation, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22Godler+DE%22">Godler DE</searchLink>; Diagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Victoria, Australia.; Department of Paediatrics, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Parkville, Victoria, Australia.
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  Data: <searchLink fieldCode="JN" term="%22101235741%22">American journal of medical genetics. Part A</searchLink> [Am J Med Genet A] 2023 Feb; Vol. 191 (2), pp. 357-369. <i>Date of Electronic Publication: </i>2022 Nov 08.
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