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- [41] FMR1 gene expression in olfactory neuroblasts from two males with fragile X syndromeAMERICAN JOURNAL OF MEDICAL GENETICS, 1999, 82 (01): : 25 - 30Abrams, MT论文数: 0 引用数: 0 h-index: 0机构: Kennedy Krieger Inst, Behav Neurogenet & Neuroimaging Res Ctr, Baltimore, MD 21201 USAKaufmann, WE论文数: 0 引用数: 0 h-index: 0机构: Kennedy Krieger Inst, Behav Neurogenet & Neuroimaging Res Ctr, Baltimore, MD 21201 USARousseau, F论文数: 0 引用数: 0 h-index: 0机构: Kennedy Krieger Inst, Behav Neurogenet & Neuroimaging Res Ctr, Baltimore, MD 21201 USAOostra, BA论文数: 0 引用数: 0 h-index: 0机构: Kennedy Krieger Inst, Behav Neurogenet & Neuroimaging Res Ctr, Baltimore, MD 21201 USAWolozin, B论文数: 0 引用数: 0 h-index: 0机构: Kennedy Krieger Inst, Behav Neurogenet & Neuroimaging Res Ctr, Baltimore, MD 21201 USATaylor, CV论文数: 0 引用数: 0 h-index: 0机构: Kennedy Krieger Inst, Behav Neurogenet & Neuroimaging Res Ctr, Baltimore, MD 21201 USALishaa, N论文数: 0 引用数: 0 h-index: 0机构: Kennedy Krieger Inst, Behav Neurogenet & Neuroimaging Res Ctr, Baltimore, MD 21201 USAMorel, ML论文数: 0 引用数: 0 h-index: 0机构: Kennedy Krieger Inst, Behav Neurogenet & Neuroimaging Res Ctr, Baltimore, MD 21201 USAHoogeveen, A论文数: 0 引用数: 0 h-index: 0机构: Kennedy Krieger Inst, Behav Neurogenet & Neuroimaging Res Ctr, Baltimore, MD 21201 USAReiss, AL论文数: 0 引用数: 0 h-index: 0机构: Kennedy Krieger Inst, Behav Neurogenet & Neuroimaging Res Ctr, Baltimore, MD 21201 USA
- [42] X-chromosome terminal deletion including the FMR1 gene in a family with fragile X-syndrome and a full mutation.MEDICINE, 2020, 99 (09)Goncalves, Liliana论文数: 0 引用数: 0 h-index: 0机构: CGC Genet, Unilabs, Lab Diagnost Mol & Genom Clin, Porto, Portugal CGC Genet, Unilabs, Lab Diagnost Mol & Genom Clin, Porto, PortugalLameiras, Ligia论文数: 0 引用数: 0 h-index: 0机构: CGC Genet, Unilabs, Lab Diagnost Mol & Genom Clin, Porto, Portugal CGC Genet, Unilabs, Lab Diagnost Mol & Genom Clin, Porto, PortugalTeixeira, Marisa论文数: 0 引用数: 0 h-index: 0机构: CGC Genet, Unilabs, Lab Diagnost Mol & Genom Clin, Porto, Portugal CGC Genet, Unilabs, Lab Diagnost Mol & Genom Clin, Porto, PortugalCerqueira, Rita论文数: 0 引用数: 0 h-index: 0机构: CGC Genet, Unilabs, Lab Diagnost Mol & Genom Clin, Porto, Portugal CGC Genet, Unilabs, Lab Diagnost Mol & Genom Clin, Porto, PortugalKay, Teresa论文数: 0 引用数: 0 h-index: 0机构: Hosp Divino Espirito Santo Ponta Delgada, EPE, Ponta Delgada, Portugal CGC Genet, Unilabs, Lab Diagnost Mol & Genom Clin, Porto, PortugalPinto-Basto, Jorge论文数: 0 引用数: 0 h-index: 0机构: CGC Genet, Unilabs, Lab Diagnost Mol & Genom Clin, Porto, Portugal CGC Genet, Unilabs, Lab Diagnost Mol & Genom Clin, Porto, Portugal
- [43] Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic featuresMOLECULAR AUTISM, 2019, 10 (1)Baker, Emma K.论文数: 0 引用数: 0 h-index: 0机构: Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, 50 Flemington Rd, Parkville, Vic 3052, Australia Univ Melbourne, Fac Med Dent & Hlth Sci, Dept Paediat, Parkville, Vic, Australia Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, 50 Flemington Rd, Parkville, Vic 3052, Australia论文数: 引用数: h-index:机构:Aliaga, Solange M.论文数: 0 引用数: 0 h-index: 0机构: Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, 50 Flemington Rd, Parkville, Vic 3052, Australia Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, 50 Flemington Rd, Parkville, Vic 3052, AustraliaBretherton, Lesley论文数: 0 引用数: 0 h-index: 0机构: Royal Childrens Hosp, Murdoch Childrens Res Inst, Brain & Mind, Melbourne, Vic, Australia Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, 50 Flemington Rd, Parkville, Vic 3052, AustraliaKraan, Claudine M.论文数: 0 引用数: 0 h-index: 0机构: Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, 50 Flemington Rd, Parkville, Vic 3052, Australia Univ Melbourne, Fac Med Dent & Hlth Sci, Dept Paediat, Parkville, Vic, Australia Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, 50 Flemington Rd, Parkville, Vic 3052, AustraliaMinh Bui论文数: 0 引用数: 0 h-index: 0机构: Univ Melbourne, Melbourne Sch Populat & Global Hlth, Ctr Epidemiol & Biostat, Carlton, Vic, Australia Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, 50 Flemington Rd, Parkville, Vic 3052, AustraliaSlater, Howard R.论文数: 0 引用数: 0 h-index: 0机构: Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, 50 Flemington Rd, Parkville, Vic 3052, Australia Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, 50 Flemington Rd, Parkville, Vic 3052, AustraliaLing, Ling论文数: 0 引用数: 0 h-index: 0机构: Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, 50 Flemington Rd, Parkville, Vic 3052, Australia Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, 50 Flemington Rd, Parkville, Vic 3052, AustraliaFrancis, David论文数: 0 引用数: 0 h-index: 0机构: Royal Childrens Hosp, Victorian Clin Genet Serv, Melbourne, Vic, Australia Royal Childrens Hosp, Murdoch Childrens Res Inst, Melbourne, Vic, Australia Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, 50 Flemington Rd, Parkville, Vic 3052, AustraliaHunter, Matthew F.论文数: 0 引用数: 0 h-index: 0机构: Monash Hlth, Monash Genet, Melbourne, Vic, Australia Monash Univ, Dept Paediat, Clayton, Vic, Australia Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, 50 Flemington Rd, Parkville, Vic 3052, AustraliaElliott, Justine论文数: 0 引用数: 0 h-index: 0机构: Royal Childrens Hosp, Victorian Clin Genet Serv, Melbourne, Vic, Australia Royal Childrens Hosp, Murdoch Childrens Res Inst, Melbourne, Vic, Australia Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, 50 Flemington Rd, Parkville, Vic 3052, AustraliaRogers, Carolyn论文数: 0 引用数: 0 h-index: 0机构: Hunter Genet, Genet Learning Disabil Serv, Waratah, NSW, Australia Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, 50 Flemington Rd, Parkville, Vic 3052, AustraliaField, Michael论文数: 0 引用数: 0 h-index: 0机构: Hunter Genet, Genet Learning Disabil Serv, Waratah, NSW, Australia Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, 50 Flemington Rd, Parkville, Vic 3052, AustraliaCohen, Jonathan论文数: 0 引用数: 0 h-index: 0机构: Fragile X Alliance Inc, North Caulfield, Vic, Australia Monash Univ, Ctr Dev Disabil Hlth Victoria, Clayton, Vic, Australia Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, 50 Flemington Rd, Parkville, Vic 3052, AustraliaCornish, Kim论文数: 0 引用数: 0 h-index: 0机构: Monash Univ, Monash Inst Cognit & Clin Neurosci, Clayton, Vic, Australia Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, 50 Flemington Rd, Parkville, Vic 3052, AustraliaSanta Maria, Lorena论文数: 0 引用数: 0 h-index: 0机构: Univ Chile, INTA, Mol & Cytogenet Lab, Santiago, Chile Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, 50 Flemington Rd, Parkville, Vic 3052, AustraliaFaundes, Victor论文数: 0 引用数: 0 h-index: 0机构: Univ Chile, INTA, Mol & Cytogenet Lab, Santiago, Chile Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, 50 Flemington Rd, Parkville, Vic 3052, AustraliaCurotto, Bianca论文数: 0 引用数: 0 h-index: 0机构: Univ Chile, INTA, Mol & Cytogenet Lab, Santiago, Chile Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, 50 Flemington Rd, Parkville, Vic 3052, AustraliaMorales, Paulina论文数: 0 引用数: 0 h-index: 0机构: Univ Chile, INTA, Mol & Cytogenet Lab, Santiago, Chile Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, 50 Flemington Rd, Parkville, Vic 3052, AustraliaTrigo, Cesar论文数: 0 引用数: 0 h-index: 0机构: Univ Chile, INTA, Mol & Cytogenet Lab, Santiago, Chile Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, 50 Flemington Rd, Parkville, Vic 3052, AustraliaSalas, Isabel论文数: 0 引用数: 0 h-index: 0机构: Univ Chile, INTA, Mol & Cytogenet Lab, Santiago, Chile Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, 50 Flemington Rd, Parkville, Vic 3052, AustraliaAlliende, Angelica M.论文数: 0 引用数: 0 h-index: 0机构: Univ Chile, INTA, Mol & Cytogenet Lab, Santiago, Chile Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, 50 Flemington Rd, Parkville, Vic 3052, Australia论文数: 引用数: h-index:机构:Godler, David E.论文数: 0 引用数: 0 h-index: 0机构: Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, 50 Flemington Rd, Parkville, Vic 3052, Australia Univ Melbourne, Fac Med Dent & Hlth Sci, Dept Paediat, Parkville, Vic, Australia Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, 50 Flemington Rd, Parkville, Vic 3052, Australia
- [44] INCOMPLETE SILENCING OF FULL MUTATION ALLELES IN MALES WITH FRAGILE X SYNDROME IS ASSOCIATED WITH AUTISTIC FEATURESJOURNAL OF INTELLECTUAL DISABILITY RESEARCH, 2019, 63 (09) : 1078 - 1078Baker, E. K.论文数: 0 引用数: 0 h-index: 0机构: Murdoch Childrens Res Inst, Diag & Dev, Parkville, Vic, Australia Univ Melbourne, Dept Paediat, Melbourne, Vic, Australia La Trobe Univ, Sch Psychol & Publ Hlth, Bundoora, Vic, Australia Murdoch Childrens Res Inst, Diag & Dev, Parkville, Vic, Australia论文数: 引用数: h-index:机构:Aliaga, S. M.论文数: 0 引用数: 0 h-index: 0机构: Murdoch Childrens Res Inst, Diag & Dev, Parkville, Vic, Australia Murdoch Childrens Res Inst, Diag & Dev, Parkville, Vic, AustraliaBretherton, L.论文数: 0 引用数: 0 h-index: 0机构: Murdoch Childrens Res Inst, Brain & Mind, Parkville, Vic, Australia Murdoch Childrens Res Inst, Diag & Dev, Parkville, Vic, AustraliaField, M.论文数: 0 引用数: 0 h-index: 0机构: Hunter Genet, Genet Learning Disabil Serv, Waratah, Australia Murdoch Childrens Res Inst, Diag & Dev, Parkville, Vic, AustraliaRogers, C.论文数: 0 引用数: 0 h-index: 0机构: Hunter Genet, Genet Learning Disabil Serv, Waratah, Australia Murdoch Childrens Res Inst, Diag & Dev, Parkville, Vic, AustraliaSanta Maria, L.论文数: 0 引用数: 0 h-index: 0机构: Univ Chile, INTA, Mol & Cytogenet Lab, Santiago, Chile Murdoch Childrens Res Inst, Diag & Dev, Parkville, Vic, AustraliaAlliende, A. M.论文数: 0 引用数: 0 h-index: 0机构: Univ Chile, INTA, Mol & Cytogenet Lab, Santiago, Chile Murdoch Childrens Res Inst, Diag & Dev, Parkville, Vic, Australia论文数: 引用数: h-index:机构:Godler, D. E.论文数: 0 引用数: 0 h-index: 0机构: Murdoch Childrens Res Inst, Diag & Dev, Parkville, Vic, Australia Univ Melbourne, Dept Paediat, Melbourne, Vic, Australia Murdoch Childrens Res Inst, Diag & Dev, Parkville, Vic, Australia
- [45] Fragile X-Associated Tremor/Ataxia Syndrome Influence of the FMR1 Gene on Motor Fiber Tracts in Males With Normal and Premutation AllelesJAMA NEUROLOGY, 2013, 70 (08) : 1022 - 1029Wang, Jun Yi论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Davis, Ctr Mind & Brain, Sacramento, CA 95817 USA Univ Calif Davis, Med Ctr, Dept Psychiat & Behav Sci, Sacramento, CA 95817 USA Univ Calif Davis, Ctr Mind & Brain, Sacramento, CA 95817 USAHessl, David论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Davis, Med Ctr, Dept Psychiat & Behav Sci, Sacramento, CA 95817 USA Univ Calif Davis, Med Ctr, Med Invest Neurodev Disorders MIND Inst, Sacramento, CA 95817 USA Univ Calif Davis, Ctr Mind & Brain, Sacramento, CA 95817 USASchneider, Andrea论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Davis, Med Ctr, Dept Pediat, Sacramento, CA 95817 USA Univ Calif Davis, Med Ctr, Med Invest Neurodev Disorders MIND Inst, Sacramento, CA 95817 USA Univ Calif Davis, Ctr Mind & Brain, Sacramento, CA 95817 USA论文数: 引用数: h-index:机构:Hagerman, Randi J.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Davis, Med Ctr, Dept Pediat, Sacramento, CA 95817 USA Univ Calif Davis, Med Ctr, Med Invest Neurodev Disorders MIND Inst, Sacramento, CA 95817 USA Univ Calif Davis, Ctr Mind & Brain, Sacramento, CA 95817 USARivera, Susan M.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Davis, Ctr Mind & Brain, Sacramento, CA 95817 USA Univ Calif Davis, Dept Psychol, Sacramento, CA 95817 USA Univ Calif Davis, Med Ctr, Med Invest Neurodev Disorders MIND Inst, Sacramento, CA 95817 USA Univ Calif Davis, Ctr Mind & Brain, Sacramento, CA 95817 USA
- [46] Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic featuresMolecular Autism, 10Emma K. Baker论文数: 0 引用数: 0 h-index: 0机构: Royal Children’s Hospital,Diagnosis and Development, Murdoch Children’s Research InstituteMarta Arpone论文数: 0 引用数: 0 h-index: 0机构: Royal Children’s Hospital,Diagnosis and Development, Murdoch Children’s Research InstituteSolange M. Aliaga论文数: 0 引用数: 0 h-index: 0机构: Royal Children’s Hospital,Diagnosis and Development, Murdoch Children’s Research InstituteLesley Bretherton论文数: 0 引用数: 0 h-index: 0机构: Royal Children’s Hospital,Diagnosis and Development, Murdoch Children’s Research InstituteClaudine M. Kraan论文数: 0 引用数: 0 h-index: 0机构: Royal Children’s Hospital,Diagnosis and Development, Murdoch Children’s Research InstituteMinh Bui论文数: 0 引用数: 0 h-index: 0机构: Royal Children’s Hospital,Diagnosis and Development, Murdoch Children’s Research InstituteHoward R. Slater论文数: 0 引用数: 0 h-index: 0机构: Royal Children’s Hospital,Diagnosis and Development, Murdoch Children’s Research InstituteLing Ling论文数: 0 引用数: 0 h-index: 0机构: Royal Children’s Hospital,Diagnosis and Development, Murdoch Children’s Research InstituteDavid Francis论文数: 0 引用数: 0 h-index: 0机构: Royal Children’s Hospital,Diagnosis and Development, Murdoch Children’s Research InstituteMatthew F. Hunter论文数: 0 引用数: 0 h-index: 0机构: Royal Children’s Hospital,Diagnosis and Development, Murdoch Children’s Research InstituteJustine Elliott论文数: 0 引用数: 0 h-index: 0机构: Royal Children’s Hospital,Diagnosis and Development, Murdoch Children’s Research InstituteCarolyn Rogers论文数: 0 引用数: 0 h-index: 0机构: Royal Children’s Hospital,Diagnosis and Development, Murdoch Children’s Research InstituteMichael Field论文数: 0 引用数: 0 h-index: 0机构: Royal Children’s Hospital,Diagnosis and Development, Murdoch Children’s Research InstituteJonathan Cohen论文数: 0 引用数: 0 h-index: 0机构: Royal Children’s Hospital,Diagnosis and Development, Murdoch Children’s Research InstituteKim Cornish论文数: 0 引用数: 0 h-index: 0机构: Royal Children’s Hospital,Diagnosis and Development, Murdoch Children’s Research InstituteLorena Santa Maria论文数: 0 引用数: 0 h-index: 0机构: Royal Children’s Hospital,Diagnosis and Development, Murdoch Children’s Research InstituteVictor Faundes论文数: 0 引用数: 0 h-index: 0机构: Royal Children’s Hospital,Diagnosis and Development, Murdoch Children’s Research InstituteBianca Curotto论文数: 0 引用数: 0 h-index: 0机构: Royal Children’s Hospital,Diagnosis and Development, Murdoch Children’s Research InstitutePaulina Morales论文数: 0 引用数: 0 h-index: 0机构: Royal Children’s Hospital,Diagnosis and Development, Murdoch Children’s Research InstituteCesar Trigo论文数: 0 引用数: 0 h-index: 0机构: Royal Children’s Hospital,Diagnosis and Development, Murdoch Children’s Research InstituteIsabel Salas论文数: 0 引用数: 0 h-index: 0机构: Royal Children’s Hospital,Diagnosis and Development, Murdoch Children’s Research InstituteAngelica M. Alliende论文数: 0 引用数: 0 h-index: 0机构: Royal Children’s Hospital,Diagnosis and Development, Murdoch Children’s Research InstituteDavid J. Amor论文数: 0 引用数: 0 h-index: 0机构: Royal Children’s Hospital,Diagnosis and Development, Murdoch Children’s Research InstituteDavid E. Godler论文数: 0 引用数: 0 h-index: 0机构: Royal Children’s Hospital,Diagnosis and Development, Murdoch Children’s Research Institute
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- [50] FMR1 fully expanded mutation with minimal methylation in a high functioning fragile X maleJOURNAL OF MEDICAL GENETICS, 1996, 33 (05) : 376 - 378Wang, ZM论文数: 0 引用数: 0 h-index: 0机构: UNIV NEBRASKA,MED CTR,DEPT PATHOL & MICROBIOL,OMAHA,NE 68198Taylor, AK论文数: 0 引用数: 0 h-index: 0机构: UNIV NEBRASKA,MED CTR,DEPT PATHOL & MICROBIOL,OMAHA,NE 68198Bridge, JA论文数: 0 引用数: 0 h-index: 0机构: UNIV NEBRASKA,MED CTR,DEPT PATHOL & MICROBIOL,OMAHA,NE 68198