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American Journal of Medical Genetics|April 17, 1999
Serotonin transporter gene (5-HTT) polymorphisms and compulsive buyingE J Devor, H J Magee, R M Dill-Devor, et al.American Journal of Medical Genetics|April 17, 1999
Association analysis between a Cys23Ser substitution polymorphism of the human 5-HT2c receptor gene and neuronal hyperexcitabilityJ Samochowiec, M Smolka, G Winterer, et al.American Journal of Medical Genetics|April 17, 1999
Lack of association between the hSKCa3 channel gene CAG polymorphism and schizophreniaR Joober, C Benkelfat, K Brisebois, et al.American Journal of Medical Genetics|April 17, 1999
Allelic variants of dopamine receptor D4 (DRD4) and serotonin receptor 5HT2c (HTR2c) and temperament factors: replication testsK U Kühn, K Meyer, M M Nöthen, et al.American Journal of Medical Genetics|April 17, 1999
Genetic linkage study of panic: clinical methodology and description of pedigreesA J Fyer, M M WeissmanAmerican Journal of Medical Genetics|April 17, 1999
Evaluation of a putative major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q14T Sander, H Schulz, A M Vieira-Saeker, et al.American Journal of Medical Genetics|April 20, 1999
Age-related language characteristics of children and adolescents with fragile X syndromeG S Fisch, J J Holden, N J Carpenter, et al.American Journal of Medical Genetics|April 20, 1999
Psychometric assessment of families with X-linked mental retardationT van Roosmalen, A P Smits, G H Thoonen, et al.American Journal of Medical Genetics|April 20, 1999
Deletion of 8.5 Mb, including the FMR1 gene, in a male with the fragile X syndrome phenotype and overgrowthR Parvari, S Mumm, A Galil, et al.American Journal of Medical Genetics|April 20, 1999
Fragile X syndrome and selective mutismR J Hagerman, J Hills, S Scharfenaker, et al.Pageof 854