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 TitleAuthors / EditorsDate
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Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes Delio, Maria; Guo, Tingwei; McDonald-McGinn, Donna M; Zackai, Elaine; ... Morrow, Bernice E 2013
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Adaptive strategy for the statistical analysis of connectomes Meskaldji, Djalel Eddine; Ottet, Marie-Christine; Cammoun, Leila; Hagmann, Patric Sacha; ... Morgenthaler, Stephan 2011
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The tumor suppressor gene TRC8/RNF139 is disrupted by a constitutional balanced translocation t(8;22)(q24.13;q11.21) in a young girl with dysgerminoma Gimelli, Stefania; Beri, Silvana; Drabkin, Harry A.; Gambini, Claudio; ... Gimelli, Giorgio 2009
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Abnormal cortical activation during response inhibition in 22q11.2 deletion syndrome Gothelf, Doron; Hoeft, Fumiko; Hinard, Christine; Hallmayer, J. F.; ... Reiss, A. L. 2007
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COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome Gothelf, Doron; Eliez, Stéphan; Thompson, Tracy; Hinard, Christine; ... Reiss, A. L. 2005
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Temporal perception in velo-cardio-facial syndrome Debbané, Martin; Glaser, Bronwyn; Gex-Fabry, Marianne; Eliez, Stéphan 2005
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A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22) Gill, M.; Vallada, H.; Collier, D.; Sham, P.; ... Read, C. M. 1996