Psychology GeneticsFISCH, Gene S.American journal of medical genetics. 2000, Vol 97, Num 2, issn 0148-7299, 64 p.Serial Issue

Cognitive-behavioral profiles of females with the fragile X mutationFISCH, Gene S.American journal of medical genetics. Part A. 2006, Vol 140, Num 7, pp 673-677, issn 1552-4825, 5 p.Article

Neurofibromatosis type 1NORTH, Kathryn.American journal of medical genetics. 2000, Vol 97, Num 2, pp 119-127, issn 0148-7299Article

Behavioral Phenotypes in Neurogenetic SyndromesBATTAGLIA, Agatino; FISCH, Gene S.American journal of medical genetics. Part C, Seminars in medical genetics. 2010, Vol 154, Num 4, issn 1552-4868, 100 p.Serial Issue

FMR1 gene and fragile X syndromeBARDONI, Barbara; MANDEL, Jean-Louis; FISCH, Gene S et al.American journal of medical genetics. 2000, Vol 97, Num 2, pp 153-163, issn 0148-7299Article

Advances in Understanding Behavioral Phenotypes in Neurogenetic SyndromesHARRIS, James C.American journal of medical genetics. Part C, Seminars in medical genetics. 2010, Vol 154, Num 4, pp 389-399, issn 1552-4868, 11 p.Article

The Behavioral Phenotype of Williams Syndrome: A Recognizable Pattern of NeurodevelopmentMORRIS, Colleen A.American journal of medical genetics. Part C, Seminars in medical genetics. 2010, Vol 154, Num 4, pp 427-431, issn 1552-4868, 5 p.Article

The Behavioral Phenotype of the Angelman SyndromeWILLIAMS, Charles A.American journal of medical genetics. Part C, Seminars in medical genetics. 2010, Vol 154, Num 4, pp 432-437, issn 1552-4868, 6 p.Article

Nosology and Epidemiology in Autism: Classification CountsFISCH, Gene S.American journal of medical genetics. Part C, Seminars in medical genetics. 2012, Vol 160, Num 2, pp 91-103, issn 1552-4868, 13 p.Article

Williams syndrome : From genotype through to the cognitive phenotypeDONNAI, Dian; KARMILOFF-SMITH, Annette.American journal of medical genetics. 2000, Vol 97, Num 2, pp 164-171, issn 0148-7299Article

Cognitive-Behavioral Features of Wolf-Hirschhorn Syndrome and Other Subtelomeric MicrodeletionsFISCH, Gene S; GROSSFELD, Paul; FALK, Rena et al.American journal of medical genetics. Part C, Seminars in medical genetics. 2010, Vol 154, Num 4, pp 417-426, issn 1552-4868, 10 p.Article

Mouse Models of Cognitive Disabilities in Trisomy 21 (Down Syndrome)ROUBERTOUX, Pierre L; CARLIER, Michèle.American journal of medical genetics. Part C, Seminars in medical genetics. 2010, Vol 154, Num 4, pp 400-416, issn 1552-4868, 17 p.Article

Longitudinal changes in cognitive and adaptive behavior scores in children and adolescents with the fragile X mutation or autismFISCH, Gene S; SIMENSEN, Richard J; SCHROER, R. J et al.Journal of autism and developmental disorders. 2002, Vol 32, Num 2, pp 107-114, issn 0162-3257Article

Neurobehavioral Phenotype in Prader-Willi SyndromeWHITTINGTON, Joyce; HOLLAND, Anthony.American journal of medical genetics. Part C, Seminars in medical genetics. 2010, Vol 154, Num 4, pp 438-447, issn 1552-4868, 10 p.Article

Evaluating data from behavioral analysis : visual inspection or statistical models?FISCH, Gene S.Behavioural processes. 2001, Vol 54, Num 1-3, pp 137-154, issn 0376-6357Conference Paper

Rett syndrome : Methyl-CpG-binding protein 2 mutations and phenotype-genotype correlationsAMIR, Ruthie E; ZOGHBI, Huda Y.American journal of medical genetics. 2000, Vol 97, Num 2, pp 147-152, issn 0148-7299Article

The Behavioral Phenotype of FMR1 MutationsBOYLE, Lia; KAUFMANN, Walter E.American journal of medical genetics. Part C, Seminars in medical genetics. 2010, Vol 154, Num 4, pp 469-476, issn 1552-4868, 8 p.Article

The Behavioral Phenotype of the Idic(15) SyndromeBATTAGLIA, Agatino; PARRINI, Barbara; TANCREDI, Raffaella et al.American journal of medical genetics. Part C, Seminars in medical genetics. 2010, Vol 154, Num 4, pp 448-455, issn 1552-4868, 8 p.Article

Chromosome 22q11 deletion syndrome : Update and review of the clinical features, cognitive-behavioral spectrum, and psychiatric complicationsSWILLEN, A; VOGELS, A; DEVRIENDT, K et al.American journal of medical genetics. 2000, Vol 97, Num 2, pp 128-135, issn 0148-7299Article

Cognitive-Behavioral Features of Children With Wolf-Hirschhorn Syndrome : Preliminary Report of 12 CasesFISCH, Gene S; BATTAGLIA, Agatino; PARRINI, Barbara et al.American journal of medical genetics. Part C, Seminars in medical genetics. 2008, Vol 148, Num 4, pp 252-256, issn 1552-4868, 5 p.Article

Prader-Willi and Angelman syndromes : Sister imprinted disordersCASSIDY, Suzanne B; DYKENS, Elisabeth; WILLIAMS, Charles A et al.American journal of medical genetics. 2000, Vol 97, Num 2, pp 136-146, issn 0148-7299Article

Behavior phenotype of FG syndrome : Cognition, personality, and behavior in eleven affected boysOZONOFF, Sally; WILLIAMS, Brenda J; RAUCH, Anita M et al.American journal of medical genetics. 2000, Vol 97, Num 2, pp 112-118, issn 0148-7299Article

Developmental Trajectories in Syndromes With Intellectual Disability, With a Focus on Wolf-Hirschhorn and Its Cognitive―Behavioral ProfileFISCH, Gene S; CARPENTER, Nancy; HOWARD-PEEBLES, Patricia N et al.American journal on intellectual and developmental disabilities (Print). 2012, Vol 117, Num 2, issn 1944-7515, 167-179, 181 [14 p.]Article

Autism Spectrum Features in Smith-Magenis SyndromeLAJE, Gonzalo; MORSE, Rebecca; RICHTER, William et al.American journal of medical genetics. Part C, Seminars in medical genetics. 2010, Vol 154, Num 4, pp 456-462, issn 1552-4868, 7 p.Article

Behavioral Features in Young Adults With FG Syndrome (Opitz-Kaveggia Syndrome)GRAHAM, John M; CLARK, Robin D; MOESCHLER, John B et al.American journal of medical genetics. Part C, Seminars in medical genetics. 2010, Vol 154, Num 4, pp 477-485, issn 1552-4868, 9 p.Article