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. |
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| 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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| ISSN: | 1552-4833 |
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| DOI: | 10.1002/ajmg.a.63027 |
