Reversing the Effects of Fragile X SyndromeOGREN, Marilee P; LOMBROSO, Paul J.Journal of the American Academy of Child and Adolescent Psychiatry. 2008, Vol 47, Num 8, pp 863-867, issn 0890-8567, 5 p.Article

Fragile X SyndromeWALLACE HAYES, Eriel; MATALON, Reuben.Pediatrics (Evanston). 2009, Vol 124, Num 2, pp 790-792, issn 0031-4005, 3 p.Article

Age-Dependent Structural Connectivity Effects in Fragile X PremutationJUN YI WANG; HESSL, David H; HAGERMAN, Randi J et al.Archives of neurology (Chicago). 2012, Vol 69, Num 4, pp 482-489, issn 0003-9942, 8 p.Article

Signaling defects in iPSC-derived fragile X premutation neuronsJING LIU; KOSCIELSKA, Katarzyna A; HAGERMAN, Randi J et al.Human molecular genetics (Print). 2012, Vol 21, Num 17, pp 3795-3805, issn 0964-6906, 11 p.Article

A Review of Fragile X Premutation Disorders: Expanding the Psychiatric PerspectiveBOURGEOIS, James A; COFFEY, Sarah M; GRIGSBY, Jim et al.The Journal of clinical psychiatry. 2009, Vol 70, Num 6, pp 852-862, issn 0160-6689, 11 p.Article

Prenatal Carrier Testing for Fragile X: Counseling Issues and ChallengesMUSCI, Thomas J; MOYER, Krista.Obstetrics and gynecology clinics of North America. 2010, Vol 37, Num 1, issn 0889-8545, viii, 61-70 [11 p.]Article

Fragile X syndrome: from molecular genetics to therapyHULST, C. D'; KOOY, R. F.Journal of medical genetics. 2009, Vol 46, Num 9, pp 577-584, issn 0022-2593, 8 p.Article

Speech fluency in fragile X syndromeVAN BORSEL, John; DOR, Orianne; RONDAL, Jean et al.Clinical linguistics & phonetics. 2008, Vol 22, Num 1, pp 1-11, issn 0269-9206, 11 p.Article

RNA-mediated pathogenesis in fragile X-associated disordersHUIPING TAN; HE LI; PENG JIN et al.Neuroscience letters. 2009, Vol 466, Num 2, pp 103-108, issn 0304-3940, 6 p.Article

Fragile X Syndrome : Keys to the Molecular Genetics of Synaptic PlasticityLOMBROSO, Paul J; OGREN, Marilee P.Journal of the American Academy of Child and Adolescent Psychiatry. 2008, Vol 47, Num 7, pp 736-739, issn 0890-8567, 4 p.Article

Identifying Large-Scale Brain Networks in Fragile X SyndromeHALL, Scott S; JIANG, Heidi; REISS, Allan L et al.JAMA psychiatry (Chicago, Ill. Print). 2013, Vol 70, Num 11, pp 1215-1223, issn 2168-622X, 9 p.Article

Preparation and validation of the first WHO international genetic reference panel for Fragile X syndromeHAWKINS, Malcolm; BOYLE, Jennifer; BURNS, Chris et al.European journal of human genetics. 2011, Vol 19, Num 1, pp 10-17, issn 1018-4813, 8 p.Article

Trajectories and Predictors of the Development of Very Young Boys with Fragile X SyndromeROBERTS, Jane E; MANKOWSKI, Jean B; SIDERIS, John et al.Journal of pediatric psychology. 2009, Vol 34, Num 8, pp 827-836, issn 0146-8693, 10 p.Article

Fragile X Full Mutation Alleles Composed of Few Alleles : Implications for CGG Repeat ExpansionNOLIN, Sarah L; DING, Xiao-Hua; HOUCK, George E et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 1, pp 60-65, issn 1552-4825, 6 p.Article

Delineating the Profile of Autism Spectrum Disorder Characteristics in Cornelia de Lange and Fragile X SyndromesMOSS, Joanna; OLIVER, Chris; NELSON, Lisa et al.American journal on intellectual and developmental disabilities (Print). 2013, Vol 118, Num 1, issn 1944-7515, 55-73, 75 [20 p.]Article

FRAGILE X PROTEIN EXPRESSION IS LINKED TO VISUAL FUNCTIONS IN HEALTHY MALE VOLUNTEERSKERI, S; BENEDEK, G.Neuroscience. 2011, Vol 192, pp 345-350, issn 0306-4522, 6 p.Article

Neuroanatomical Differences in Toddler Boys With Fragile X Syndrome and Idiopathic AutismHOEFT, Fumiko; WALTER, Elizabeth; LIGHTBODY, Amy A et al.Archives of general psychiatry. 2011, Vol 68, Num 3, pp 295-305, issn 0003-990X, 11 p.Article

The effect of CGG repeat number on ovarian response among fragile X premutation carriers undergoing preimplantation genetic diagnosisBIBI, Guy; MALCOV, Mira; YUVAL, Yaron et al.Fertility and sterility. 2010, Vol 94, Num 3, pp 869-874, issn 0015-0282, 6 p.Article

A Distinct DNA-Methylation Boundary in the 5'- Upstream Sequence of the FMR1 Promoter Binds Nuclear Proteins and Is Lost in Fragile X SyndromeNAUMANN, Anja; HOCHSTEIN, Norbert; WEBER, Stefanie et al.American journal of human genetics. 2009, Vol 85, Num 5, pp 606-616, issn 0002-9297, 11 p.Article

A pilot open label, single dose trial of fenobam in adults with fragile X syndromeBERRY-KRAVIS, E; HESSL, D; HAGERMAN, R et al.Journal of medical genetics. 2009, Vol 46, Num 4, pp 266-271, issn 0022-2593, 6 p.Article

Haplotype Analysis at the FRAXA Locus in an Indian PopulationSAHA CHAKRABORTY, S; BAMA CHARAN MONDAL; DAS, S et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 15, pp 1980-1985, issn 1552-4825, 6 p.Article

A Fragile X Sibship from a Consanguineous Family With a Compound Heterozygous Female and Partially Methylated Full Mutation MaleSORENSEN, Page L; BASUTA, Kirin; MENDOZA-MORALES, Guadalupe et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 5, pp 1221-1224, issn 1552-4825, 4 p.Article

Altered maturation of the primary somatosensory cortex in a mouse model of fragile X syndromeTILL, Sally M; WIJETUNGE, Lasani S; SEIDEL, Viktoria G et al.Human molecular genetics (Print). 2012, Vol 21, Num 10, pp 2143-2156, issn 0964-6906, 14 p.Article

Intermediate FMR1 alleles and cognitive and/or behavioural phenotypesMADRIGAL, Irene; XUNCLA, Mar; TEJADA, Maria Isabel et al.European journal of human genetics. 2011, Vol 19, Num 8, pp 921-923, issn 1018-4813, 3 p.Article

Parkinsonism and Cognitive Decline in a Fragile X Mosaic MaleHALL, Deborah; PICKLER, Laura; RILEY, Karen et al.Movement disorders. 2010, Vol 25, Num 10, pp 1523-1524, issn 0885-3185, 2 p.Article