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Genomics|August 1, 1993
Localization of the human tripeptidyl peptidase II gene (TPP2) to 13q32-q33 by nonradioactive in situ hybridization and somatic cell hybridsT Martinsson, M Vujic, B TomkinsonArchives of Disease in Childhood|January 23, 2004
Incidence and prevalence of the 22q11 deletion syndrome: a population-based study in Western SwedenS Oskarsdóttir, M Vujic, A FasthAmerican Journal of Human Genetics|November 1, 1995
Localization of a gene for autosomal dominant Larsen syndrome to chromosome region 3p21.1-14.1 in the proximity of, but distinct from, the COL7A1 locusM Vujic, K Hallstensson, J Wahlström, et al.European Child & Adolescent Psychiatry|December 1, 1996
Maternal origin of inv dup(15) chromosomes in infantile autismT Martinsson, T Johannesson, M Vujic, et al.Prenatal Diagnosis|November 1, 1994
Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: prevalence and characterization by fluorescence in situ hybridizationE Blennow, T H Bui, U Kristoffersson, et al.Journal of B.U.ON. : Official Journal of the Balkan Union of Oncology|April 25, 2013
Cytotoxic effects of palladium (II) and platinum (II) complexes with O,O'-dialkyl esters of (S,S)-ethylenediamine-N,N'-di-2-(4-methyl) pentanoic acid on human colon cancer cell linesV Volarevic, J M Vujic, M Milovanovic, et al.The EMBO Journal|December 18, 2001
Repression of inflammatory responses in the absence of DNA binding by the glucocorticoid receptorH M Reichardt, J P Tuckermann, M Göttlicher, et al.Journal of Medical Genetics|May 5, 1999
Congenital variant Rett syndrome in a girl with terminal deletion of chromosome 3pJ Wahlström, A Uller, T Johannesson, et al.Journal of Proteomics|May 25, 2016
Oncogenic KIT mutations in different exons lead to specific changes in melanocyte phospho-proteomeM Sanlorenzo, I Vujic, C Posch, et al.Nature Genetics|July 14, 1998
Identification of the gene responsible for Best macular dystrophyK Petrukhin, M J Koisti, B Bakall, et al.Pageof 1