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Human Genetics|January 26, 2002
Investigation of the functional effect of monoamine oxidase polymorphisms in human brainJ Balciuniene, L Emilsson, L Oreland, et al.Genomics|November 20, 1995
A gene for autosomal dominant progressive cone dystrophy (CORD5) maps to chromosome 17p12-p13J Balciuniene, K Johansson, O Sandgren, et al.Journal of Molecular Evolution|March 7, 2001
The geographic distribution of monoamine oxidase haplotypes supports a bottleneck during the dispersion of modern humans from AfricaJ Balciuniene, A C Syvänen, H L McLeod, et al.American Journal of Human Genetics|August 27, 1998
Evidence for digenic inheritance of nonsyndromic hereditary hearing loss in a Swedish familyJ Balciuniene, N Dahl, E Borg, et al.Human Genetics|September 15, 2000
Alpha-tectorin involvement in hearing disabilities: one gene--two phenotypesJ Balciuniene, N Dahl, P Jalonen, et al.Genome Research|December 1, 1996
Chromosome-specific panels of tri- and tetranucleotide microsatellite markers for multiplex fluorescent detection and automated genotyping: evaluation of their utility in pathology and forensicsA K Lindqvist, P K Magnusson, J Balciuniene, et al.American Journal of Medical Genetics|July 14, 1999
Linkage analysis of a large Swedish kindred provides further support for a susceptibility locus for schizophrenia on chromosome 6p23E Lindholm, B Ekholm, J Balciuniene, et al.Molecular Psychiatry|May 13, 1998
Linkage analysis of candidate loci in families with recurrent major depressionJ Balciuniene, Q P Yuan, C Engström, et al.Molecular Psychiatry|October 17, 1998
Two commonly expanded CAG/CTG repeat loci: involvement in affective disorders?K Lindblad, P O Nylander, C Zander, et al.Pageof 1