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- [1] Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNAAMERICAN JOURNAL OF MEDICAL GENETICS, 2000, 94 (03): : 232 - 236Tassone, F论文数: 0 引用数: 0 h-index: 0机构: Univ Colorado, Hlth Sci Ctr, Sch Med B121, Dept Biochem & Mol Genet, Denver, CO 80262 USAHagerman, RJ论文数: 0 引用数: 0 h-index: 0机构: Univ Colorado, Hlth Sci Ctr, Sch Med B121, Dept Biochem & Mol Genet, Denver, CO 80262 USALoesch, DZ论文数: 0 引用数: 0 h-index: 0机构: Univ Colorado, Hlth Sci Ctr, Sch Med B121, Dept Biochem & Mol Genet, Denver, CO 80262 USALachiewicz, A论文数: 0 引用数: 0 h-index: 0机构: Univ Colorado, Hlth Sci Ctr, Sch Med B121, Dept Biochem & Mol Genet, Denver, CO 80262 USATaylor, AK论文数: 0 引用数: 0 h-index: 0机构: Univ Colorado, Hlth Sci Ctr, Sch Med B121, Dept Biochem & Mol Genet, Denver, CO 80262 USAHagerman, PJ论文数: 0 引用数: 0 h-index: 0机构: Univ Colorado, Hlth Sci Ctr, Sch Med B121, Dept Biochem & Mol Genet, Denver, CO 80262 USA
- [2] Fragile X Syndrome in a Female With Homozygous Full-Mutation Alleles of the FMR1 GeneCUREUS JOURNAL OF MEDICAL SCIENCE, 2021, 13 (07)Vafaeie, Farzane论文数: 0 引用数: 0 h-index: 0机构: Genet Fdn Khorasan Razavi, Med Genet Lab, Mashhad, Razavi Khorasan, Iran Genet Fdn Khorasan Razavi, Med Genet Lab, Mashhad, Razavi Khorasan, IranAlerasool, Masoome论文数: 0 引用数: 0 h-index: 0机构: Genet Fdn Khorasan Razavi, Med Genet Lab, Mashhad, Razavi Khorasan, Iran Mashhad Univ Med Sci, Dept Med Genet, Mashhad, Razavi Khorasan, Iran Genet Fdn Khorasan Razavi, Med Genet Lab, Mashhad, Razavi Khorasan, IranMojaver, Nasrin Kaseb论文数: 0 引用数: 0 h-index: 0机构: Genet Fdn Khorasan Razavi, Med Genet Lab, Mashhad, Razavi Khorasan, Iran Genet Fdn Khorasan Razavi, Med Genet Lab, Mashhad, Razavi Khorasan, IranMojarrad, Majid论文数: 0 引用数: 0 h-index: 0机构: Genet Fdn Khorasan Razavi, Med Genet Lab, Mashhad, Razavi Khorasan, Iran Mashhad Univ Med Sci, Dept Med Genet, Mashhad, Razavi Khorasan, Iran Mashhad Univ Med Sci, Genet Res Ctr, Fac Med, Mashhad, Razavi Khorasan, Iran Genet Fdn Khorasan Razavi, Med Genet Lab, Mashhad, Razavi Khorasan, Iran
- [3] FMR1 mRNA from full mutation alleles is associated with ABC-CFX scores in males with fragile X syndromeSCIENTIFIC REPORTS, 2020, 10 (01)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, Dept Paediat, Fac Med Dent & Hlth Sci, Parkville, Vic, Australia La Trobe Univ, Sch Psychol & Publ Hlth, Bundoora, 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:Kraan, Claudine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, Dept Paediat, Fac Med Dent & Hlth Sci, 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, AustraliaRogers, Carolyn论文数: 0 引用数: 0 h-index: 0机构: Hunter New England Hlth, Genet Learning Disabil Serv, Hunter Genet, 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 New England Hlth, Genet Learning Disabil Serv, Hunter Genet, Waratah, NSW, 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, 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, AustraliaUre, Alexandra论文数: 0 引用数: 0 h-index: 0机构: Univ Melbourne, Dept Paediat, Fac Med Dent & Hlth Sci, Parkville, Vic, Australia Royal Childrens Hosp, Murdoch Childrens Res Inst, Neurodisabil & Rehabil, Melbourne, Vic, Australia Royal Childrens Hosp, Melbourne, Vic, Australia Monash Univ, Dept Pediat, Clayton, Vic, 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, AustraliaHunter, Matthew F.论文数: 0 引用数: 0 h-index: 0机构: Monash Hlth, Monash Genet, 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, Inst Nutr & Food Technol INTA, Dept Genet & Metab Dis, Lab Mol Cytogenet, 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, Inst Nutr & Food Technol INTA, Dept Genet & Metab Dis, Lab Mol Cytogenet, 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, Inst Nutr & Food Technol INTA, Dept Genet & Metab Dis, Lab Mol Cytogenet, 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, Inst Nutr & Food Technol INTA, Dept Genet & Metab Dis, Lab Mol Cytogenet, 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, Inst Nutr & Food Technol INTA, Dept Genet & Metab Dis, Lab Mol Cytogenet, 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, Inst Nutr & Food Technol INTA, Dept Genet & Metab Dis, Lab Mol Cytogenet, Santiago, Chile Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, 50 Flemington Rd, Parkville, Vic 3052, AustraliaAlliende, Angelica论文数: 0 引用数: 0 h-index: 0机构: Univ Chile, Inst Nutr & Food Technol INTA, Dept Genet & Metab Dis, Lab Mol Cytogenet, 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, Dept Paediat, Fac Med Dent & Hlth Sci, Parkville, Vic, Australia Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, 50 Flemington Rd, Parkville, Vic 3052, Australia
- [4] FMR1 mRNA from full mutation alleles is associated with ABC-CFX scores in males with fragile X syndromeScientific Reports, 10Emma K. Baker论文数: 0 引用数: 0 h-index: 0机构: Murdoch Children’s Research Institute,Diagnosis and DevelopmentMarta Arpone论文数: 0 引用数: 0 h-index: 0机构: Murdoch Children’s Research Institute,Diagnosis and DevelopmentClaudine Kraan论文数: 0 引用数: 0 h-index: 0机构: Murdoch Children’s Research Institute,Diagnosis and DevelopmentMinh Bui论文数: 0 引用数: 0 h-index: 0机构: Murdoch Children’s Research Institute,Diagnosis and DevelopmentCarolyn Rogers论文数: 0 引用数: 0 h-index: 0机构: Murdoch Children’s Research Institute,Diagnosis and DevelopmentMichael Field论文数: 0 引用数: 0 h-index: 0机构: Murdoch Children’s Research Institute,Diagnosis and DevelopmentLesley Bretherton论文数: 0 引用数: 0 h-index: 0机构: Murdoch Children’s Research Institute,Diagnosis and DevelopmentLing Ling论文数: 0 引用数: 0 h-index: 0机构: Murdoch Children’s Research Institute,Diagnosis and DevelopmentAlexandra Ure论文数: 0 引用数: 0 h-index: 0机构: Murdoch Children’s Research Institute,Diagnosis and DevelopmentJonathan Cohen论文数: 0 引用数: 0 h-index: 0机构: Murdoch Children’s Research Institute,Diagnosis and DevelopmentMatthew F. Hunter论文数: 0 引用数: 0 h-index: 0机构: Murdoch Children’s Research Institute,Diagnosis and DevelopmentLorena Santa María论文数: 0 引用数: 0 h-index: 0机构: Murdoch Children’s Research Institute,Diagnosis and DevelopmentVictor Faundes论文数: 0 引用数: 0 h-index: 0机构: Murdoch Children’s Research Institute,Diagnosis and DevelopmentBianca Curotto论文数: 0 引用数: 0 h-index: 0机构: Murdoch Children’s Research Institute,Diagnosis and DevelopmentPaulina Morales论文数: 0 引用数: 0 h-index: 0机构: Murdoch Children’s Research Institute,Diagnosis and DevelopmentCesar Trigo论文数: 0 引用数: 0 h-index: 0机构: Murdoch Children’s Research Institute,Diagnosis and DevelopmentIsabel Salas论文数: 0 引用数: 0 h-index: 0机构: Murdoch Children’s Research Institute,Diagnosis and DevelopmentAngelica Alliende论文数: 0 引用数: 0 h-index: 0机构: Murdoch Children’s Research Institute,Diagnosis and DevelopmentDavid J. Amor论文数: 0 引用数: 0 h-index: 0机构: Murdoch Children’s Research Institute,Diagnosis and DevelopmentDavid E. Godler论文数: 0 引用数: 0 h-index: 0机构: Murdoch Children’s Research Institute,Diagnosis and Development
- [5] Significantly Elevated FMR1 mRNA and Mosaicism for Methylated Premutation and Full Mutation Alleles in Two Brothers with Autism Features Referred for Fragile X TestingINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2019, 20 (16)Field, Michael论文数: 0 引用数: 0 h-index: 0机构: Hunter Genet, Genet Learning Disabil Serv, Waratah, NSW 2298, Australia Hunter Genet, Genet Learning Disabil Serv, Waratah, NSW 2298, Australia论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构: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, Parkville, Vic 3052, Australia Univ Melbourne, Fac Med Dent & Hlth Sci, Dept Paediat, Parkville, Vic 3052, Australia La Trobe Univ, Sch Psychol & Publ Hlth, Bundoora, Vic 3086, Australia Hunter Genet, Genet Learning Disabil Serv, Waratah, NSW 2298, AustraliaAliaga, Solange M.论文数: 0 引用数: 0 h-index: 0机构: Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, Parkville, Vic 3052, Australia Univ Melbourne, Fac Med Dent & Hlth Sci, Dept Paediat, Parkville, Vic 3052, Australia Hunter Genet, Genet Learning Disabil Serv, Waratah, NSW 2298, AustraliaRogers, Carolyn论文数: 0 引用数: 0 h-index: 0机构: Hunter Genet, Genet Learning Disabil Serv, Waratah, NSW 2298, Australia Hunter Genet, Genet Learning Disabil Serv, Waratah, NSW 2298, AustraliaHickerton, Chriselle论文数: 0 引用数: 0 h-index: 0机构: Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, Parkville, Vic 3052, Australia Hunter Genet, Genet Learning Disabil Serv, Waratah, NSW 2298, AustraliaFrancis, David论文数: 0 引用数: 0 h-index: 0机构: Royal Childrens Hosp, Murdoch Childrens Res Inst, Victorian Clin Genet Serv, Parkville, Vic 3052, Australia Hunter Genet, Genet Learning Disabil Serv, Waratah, NSW 2298, AustraliaPhelan, Dean G.论文数: 0 引用数: 0 h-index: 0机构: Royal Childrens Hosp, Murdoch Childrens Res Inst, Victorian Clin Genet Serv, Parkville, Vic 3052, Australia Hunter Genet, Genet Learning Disabil Serv, Waratah, NSW 2298, AustraliaPalmer, Elizabeth E.论文数: 0 引用数: 0 h-index: 0机构: Hunter Genet, Genet Learning Disabil Serv, Waratah, NSW 2298, Australia Hunter Genet, Genet Learning Disabil Serv, Waratah, NSW 2298, Australia论文数: 引用数: h-index:机构:Slater, Howard论文数: 0 引用数: 0 h-index: 0机构: Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, Parkville, Vic 3052, Australia Univ Melbourne, Fac Med Dent & Hlth Sci, Dept Paediat, Parkville, Vic 3052, Australia Royal Childrens Hosp, Murdoch Childrens Res Inst, Victorian Clin Genet Serv, Parkville, Vic 3052, Australia Hunter Genet, Genet Learning Disabil Serv, Waratah, NSW 2298, AustraliaBretherton, Lesley论文数: 0 引用数: 0 h-index: 0机构: Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, Parkville, Vic 3052, Australia Univ Melbourne, Fac Med Dent & Hlth Sci, Dept Paediat, Parkville, Vic 3052, Australia Royal Childrens Hosp, Psychol Serv, Parkville, Vic 3052, Australia Univ Melbourne, Melbourne Sch Psychol Sci, Parkville, Vic 3052, Australia Hunter Genet, Genet Learning Disabil Serv, Waratah, NSW 2298, AustraliaLing, Ling论文数: 0 引用数: 0 h-index: 0机构: Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, Parkville, Vic 3052, Australia Hunter Genet, Genet Learning Disabil Serv, Waratah, NSW 2298, AustraliaGodler, David E.论文数: 0 引用数: 0 h-index: 0机构: Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, Parkville, Vic 3052, Australia Univ Melbourne, Fac Med Dent & Hlth Sci, Dept Paediat, Parkville, Vic 3052, Australia Hunter Genet, Genet Learning Disabil Serv, Waratah, NSW 2298, Australia
- [6] Postmortem examination of two fragile X brothers with an FMR1 full mutationAMERICAN JOURNAL OF MEDICAL GENETICS, 1999, 84 (03): : 245 - 249Reyniers, E论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Dept Med Genet, B-2610 Antwerp, BelgiumMartin, JJ论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Dept Med Genet, B-2610 Antwerp, BelgiumCras, P论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Dept Med Genet, B-2610 Antwerp, BelgiumVan Marck, E论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Dept Med Genet, B-2610 Antwerp, BelgiumHandig, I论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Dept Med Genet, B-2610 Antwerp, BelgiumJorens, HZJ论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Dept Med Genet, B-2610 Antwerp, BelgiumOostra, BA论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Dept Med Genet, B-2610 Antwerp, BelgiumKooy, RF论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Dept Med Genet, B-2610 Antwerp, BelgiumWillems, PJ论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Dept Med Genet, B-2610 Antwerp, Belgium
- [7] Abnormally Methylated FMR1 in Absence of a Detectable Full Mutation in a USA Patient Cohort Referred for Fragile X TestingSCIENTIFIC REPORTS, 2019, 9 (1)Hensel, Charles H.论文数: 0 引用数: 0 h-index: 0机构: Lineagen Inc, Salt Lake City, UT USA Lineagen Inc, Salt Lake City, UT USAVanzo, Rena J.论文数: 0 引用数: 0 h-index: 0机构: Lineagen Inc, Salt Lake City, UT USA Lineagen Inc, Salt Lake City, UT USAMartin, Megan M.论文数: 0 引用数: 0 h-index: 0机构: Lineagen Inc, Salt Lake City, UT USA Lineagen Inc, Salt Lake City, UT USALing, Ling论文数: 0 引用数: 0 h-index: 0机构: Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, Melbourne, Vic, Australia Lineagen Inc, Salt Lake City, UT USAAliaga, Solange M.论文数: 0 引用数: 0 h-index: 0机构: Royal Childrens Hosp, Murdoch Childrens Res Inst, Diag & Dev, Melbourne, Vic, Australia Lineagen Inc, Salt Lake City, UT USABui, Minh论文数: 0 引用数: 0 h-index: 0机构: Univ Melbourne, Ctr Epidemiol & Biostat, Melbourne Sch Populat & Global Hlth, Melbourne, Vic, Australia Lineagen Inc, Salt Lake City, UT USAFrancis, David, I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 Lineagen Inc, Salt Lake City, UT USATwede, Hope论文数: 0 引用数: 0 h-index: 0机构: Lineagen Inc, Salt Lake City, UT USA Lineagen Inc, Salt Lake City, UT USAField, Michael H.论文数: 0 引用数: 0 h-index: 0机构: GOLD Serv, Hunter Genet, Newcastle, NSW, Australia Lineagen Inc, Salt Lake City, UT USAMorison, Jonathon W.论文数: 0 引用数: 0 h-index: 0机构: Royal Childrens Hosp, Murdoch Childrens Res Inst, Business Dev & Legal Off, Melbourne, Vic, Australia Lineagen Inc, Salt Lake City, UT USA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, Melbourne, Vic, Australia Univ Melbourne, Dept Paediat, Fac Med Dent & Hlth Sci, Parkville, Vic, Australia Lineagen Inc, Salt Lake City, UT USA
- [8] Fragile X syndrome in a male with methylated premutation alleles and no detectable methylated full mutation allelesAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2019, 179 (10) : 2132 - 2137Hayward, Bruce论文数: 0 引用数: 0 h-index: 0机构: NIDDK, Sect Gene Struct & Dis, Lab Cell & Mol Biol, NIH, Bethesda, MD 20892 USA NIMH, Sect Neuroadaptat & Prot Metab, NIH, Bethesda, MD 20892 USALoutaev, Inna论文数: 0 引用数: 0 h-index: 0机构: NIMH, Sect Neuroadaptat & Prot Metab, NIH, Bethesda, MD 20892 USA NIMH, Sect Neuroadaptat & Prot Metab, NIH, Bethesda, MD 20892 USADing, Xiaohua论文数: 0 引用数: 0 h-index: 0机构: New York State Inst Basic Res Dev Disabil, Mol Diagnost Lab, 1050 Forest Hill Rd, Staten Isl, NY 10314 USA NIMH, Sect Neuroadaptat & Prot Metab, NIH, Bethesda, MD 20892 USANolin, Sarah L.论文数: 0 引用数: 0 h-index: 0机构: New York State Inst Basic Res Dev Disabil, Mol Diagnost Lab, 1050 Forest Hill Rd, Staten Isl, NY 10314 USA NIMH, Sect Neuroadaptat & Prot Metab, NIH, Bethesda, MD 20892 USAThurm, Audrey论文数: 0 引用数: 0 h-index: 0机构: NIMH, Off Clin Director, NIH, Bethesda, MD 20892 USA NIMH, Sect Neuroadaptat & Prot Metab, NIH, Bethesda, MD 20892 USAUsdin, Karen论文数: 0 引用数: 0 h-index: 0机构: NIDDK, Sect Gene Struct & Dis, Lab Cell & Mol Biol, NIH, Bethesda, MD 20892 USA NIMH, Sect Neuroadaptat & Prot Metab, NIH, Bethesda, MD 20892 USASmith, Carolyn B.论文数: 0 引用数: 0 h-index: 0机构: NIMH, Sect Neuroadaptat & Prot Metab, NIH, Bethesda, MD 20892 USA NIMH, Sect Neuroadaptat & Prot Metab, NIH, Bethesda, MD 20892 USA
- [9] Mosaicism for FMR1 gene full mutation and deletion in a fragile X female.AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (05) : 585 - 585Fan, H论文数: 0 引用数: 0 h-index: 0机构: Univ N Carolina, Chapel Hill, NC USABooker, JK论文数: 0 引用数: 0 h-index: 0机构: Univ N Carolina, Chapel Hill, NC USAMcCandless, SE论文数: 0 引用数: 0 h-index: 0机构: Univ N Carolina, Chapel Hill, NC USAShashi, V论文数: 0 引用数: 0 h-index: 0机构: Univ N Carolina, Chapel Hill, NC USAFarber, RA论文数: 0 引用数: 0 h-index: 0机构: Univ N Carolina, Chapel Hill, NC USA
- [10] A nonsense mutation in FMR1 causing fragile X syndromeEuropean Journal of Human Genetics, 2011, 19 : 489 - 491Karen Grønskov论文数: 0 引用数: 0 h-index: 0机构: Center for Applied Human Molecular Genetics,Karen Brøndum-Nielsen论文数: 0 引用数: 0 h-index: 0机构: Center for Applied Human Molecular Genetics,Alma Dedic论文数: 0 引用数: 0 h-index: 0机构: Center for Applied Human Molecular Genetics,Helle Hjalgrim论文数: 0 引用数: 0 h-index: 0机构: Center for Applied Human Molecular Genetics,