Authors: Tentler, D Brandberg, G Betancur, C Gillberg, C Anneren, G Orsmark, C Green, ED Carlsson, B Dahl, N

Citation: D. Tentler et al., A balanced reciprocal translocation t(5;7)(q14;q32) associated with autistic disorder: Molecular analysis of the chromosome 7 breakpoint, AM J MED G, 105(8), 2001, pp. 729-736

Authors: Schueler, MG Higgins, AW Nagaraja, R Tentler, D Dahl, N Gustashaw, K Willard, HF

Citation: Mg. Schueler et al., Large-insert clone/STS contigs in Xq11-q12, spanning deletions in patientswith androgen insensitivity and mental retardation, GENOMICS, 66(1), 2000, pp. 104-109

Authors: Tentler, D Gustavsson, P Elinder, G Eklof, O Gordon, L Mandel, A Dahl, N

Citation: D. Tentler et al., A microdeletion in 19q13.2 associated with mental retardation, skeletal malformations, and Diamond-Blackfan anaemia suggests a novel contiguous gene syndrome, J MED GENET, 37(2), 2000, pp. 128-131

Authors: Draptchinskaia, N Gustavsson, P Andersson, B Pettersson, M Willig, TN Dianzani, I Ball, S Tchernia, G Klar, J Matsson, H Tentler, D Mohandas, N Carlsson, B Dahl, N

Citation: N. Draptchinskaia et al., The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia, NAT GENET, 21(2), 1999, pp. 169-175

Authors: Tentler, D Gustavsson, P Leisti, J Schueler, M Chelly, J Timonen, E Anneren, G Willard, HF Dahl, N

Citation: D. Tentler et al., Deletion including the oligophrenin-1 gene associated with enlarged cerebral ventricles, cerebellar hypoplasia, seizures and ataxia, EUR J HUM G, 7(5), 1999, pp. 541-548