Modeling Family Adaptation to Fragile X SyndromeRASPA, Melissa; BAILEY, Donald B; BANN, Carla et al.American journal on intellectual and developmental disabilities (Print). 2014, Vol 119, Num 1, issn 1944-7515, 33-48, 100, 102 [18 p.]Article

Pharmacological Rescue of Cortical Synaptic and Network Potentiation in a Mouse Model for Fragile X SyndromeTAO CHEN; LU, Jing-Shan; QIAN SONG et al.Neuropsychopharmacology (New York, NY). 2014, Vol 39, Num 8, pp 1955-1967, issn 0893-133X, 13 p.Article

Social Approach and Emotion Recognition in Fragile X SyndromeWILLIAMS, Tracey A; PORTER, Melanie A; LANGDON, Robyn et al.American journal on intellectual and developmental disabilities (Print). 2014, Vol 119, Num 2, issn 1944-7515, 133-150, 199, 201 [20 p.]Article

The FMR1 Gene and Fragile X-Associated Tremor/Ataxia SyndromeBROUWER, J. R; WILLEMSEN, R; OOSTRA, B. A et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2009, Vol 150, Num 6, pp 782-798, issn 1552-4841, 17 p.Article

A Girl With Fragile X Premutation From Sperm DonationWIROJANAN, Juthamas; ANGKUSTSIRI, Kathleen; TASSONE, Flora et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 7, pp 888-892, issn 1552-4825, 5 p.Article

Child and Genetic Variables Associated With Maternal Adaptation to Fragile X Syndrome : A Multidimensional AnalysisBAILEY, Donald B; SIDERIS, John; ROBERTS, Jane et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 6, pp 720-729, issn 1552-4825, 10 p.Article

Wild-Type Male Offspring of fmr-I ^+/-Mothers Exhibit Characteristics of the Fragile X PhenotypeZUPAN, Bojana; TOTH, Miklos.Neuropsychopharmacology (New York, NY). 2008, Vol 33, Num 11, pp 2667-2675, issn 0893-133X, 9 p.Article

Sustained attention and response inhibition in boys with fragile X syndrome : Measures of continuous performanceSULLIVAN, Kelly; HATTON, Deborah D; HAMMER, Julie et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2007, Vol 144, Num 4, pp 517-532, issn 1552-4841, 16 p.Article

Oxidative stress reveals heterogeneity of FMRP granules in PC12 cell neuritesDOLZHANSKAYA, Natalia; MERZ, George; DENMAN, Robert B et al.Brain research. 2006, Vol 1112, pp 56-64, issn 0006-8993, 9 p.Article

Decreased expression of the GABA_A receptor in fragile X syndromeD'HULST, Charlotte; DE GEEST, Natalie; REEUE, Simon P et al.Brain research. 2006, Vol 1121, pp 238-245, issn 0006-8993, 8 p.Article

The FMRP BCI RNA Controversy : Tempest in a teapot or symptomatic of a larger problem?DENMAN, Robert B.The molecular basis of fragile X syndrome. 2005, pp 65-79, isbn 81-7736-257-7, 1Vol, 15 p.Book Chapter

Sculpting the brain - : The role of FMRP in synaptic plasticityREIS, Surya A; OOSTRA, Ben A; WILLEMSEN, Rob et al.The molecular basis of fragile X syndrome. 2005, pp 145-169, isbn 81-7736-257-7, 1Vol, 25 p.Book Chapter

Five years of molecular diagnosis of Fragile X syndrome (1997-2001): A collaborative study reporting 95% of the activity in FranceBIANCALANA, Valérie; BELDJORD, Chérif; TAILLANDIER, Agnès et al.American journal of medical genetics. 2004, Vol 129A, Num 3, pp 218-224, issn 0148-7299, 7 p.Article

Telomere dynamics in fancg-deficient mouse and human cellsFRANCO, Sonia; VAN DE VRUGT, Henri J; FERNANDEZ, Piedad et al.Blood. 2004, Vol 104, Num 13, pp 3927-3935, issn 0006-4971, 9 p.Article

The fragile genes FHIT and WWOX are inactivated coordinately in invasive breast carcinoma: Correlations with clinical featuresGULER, Gulnur; UNER, Aysegul; GULER, Nilufer et al.Cancer. 2004, Vol 100, Num 8, pp 1605-1614, issn 0008-543X, 10 p.Conference Paper

Biological and environmental contributions to adaptive behavior in fragile X syndromeGLASER, Bronwyn; HESSL, David; DYER-FRIEDMAN, Jennifer et al.American journal of medical genetics. 2003, Vol 117A, Num 1, pp 21-29, issn 0148-7299, 9 p.Article

Concurrence of fragile X syndrome and 47, XYY in an individual with a Prader-Willi-like phenotypeSTALKER, Heather J; KELLER, Kory L; GRAY, Brian A et al.American journal of medical genetics. 2003, Vol 116A, Num 2, pp 176-178, issn 0148-7299, 3 p.Article

Cytogenetic analysis of obsessive-compulsive disorder (OCD): Identification of a FRAXE fragile siteQING WANG; YANGHONG GU; FERGUSON, James M et al.American journal of medical genetics. 2003, Vol 118A, Num 1, pp 25-28, issn 0148-7299, 4 p.Article

Fluorescent microplate-based analysis of protein-DNA interactions I: immobilized proteinZHANG, Zhan-Ren; PALFREY, David; NAGEL, David A et al.BioTechniques. 2003, Vol 35, Num 5, pp 980-986, issn 0736-6205, 4 p.Article

Mapping of MRX81 in Xp11.2-xq12 suggests the presence of a new gene involved in nonspecific X-linked mental retardationANNUNZIATA, Ida; LANZARA, Carmela; CONTE, Ivan et al.American journal of medical genetics. 2003, Vol 118A, Num 3, pp 217-222, issn 0148-7299, 6 p.Article

Tremor, ataxia and dementia in older men may indicate a carrier of the fragile X syndromeROGERS, C; PARTINGTONA, M. W; TURNER, G. M et al.Clinical genetics. 2003, Vol 64, Num 1, pp 54-56, issn 0009-9163, 3 p.Article

Fanconi anemia type C-deficient hematopoietic stem/progenitor cells exhibit aberrant cell cycle controlXIAXIN LI; PLETT, P. Artur; YANZHU YANG et al.Blood. 2003, Vol 102, Num 6, pp 2081-2084, issn 0006-4971, 4 p.Article

Le syndrome de l'X fragile, pourquoi le rechercher, quand faut-il y penser ? = Fragile X syndromeGERARD-BLANLUET, Marion.MTP. Médecine thérapeutique pédiatrie. 2003, Vol 6, Num 2, pp 58-65, issn 1286-5494, 8 p.Article

Point and interval estimations of circadian melatonin ecphasia in Smith-Magenis syndromeCORNELISSEN, Germaine; HALBERG, Franz; TARQUINI, Roberto et al.Biomedicine & pharmacotherapy. 2003, Vol 57, pp 31s-34s, issn 0753-3322, SUP1Conference Paper

Alterations in the auditory startle response in Fmr1 targeted mutant mouse models of fragile X syndromeNIELSEN, Darci M; DERBER, William J; MCCLELLAN, Danielle A et al.Brain research. 2002, Vol 927, Num 1, pp 8-17, issn 0006-8993Article