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Clinical Genetics|March 1, 1990
High resolution banding of an unusual reciprocal translocation in recurrent abortionsP M Kroisel, W RosenkranzFortschritte Der Neurologie-Psychiatrie|November 5, 2005
[Genetic risk factors in schizophrenia]H Fabisch, P M Kroisel, Karin FabischMammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1992
Localization of genes and anonymous DNA probes on the short arm of chromosome 7K Wagner, P M Kroisel, W RosenkranzClinical Genetics|December 8, 1998
Isolation of a 370 kb YAC fragment spanning a translocation breakpoint at 3p14.1 associated with holoprosencephalyE Petek, P M Kroisel, K WagnerGenomics|November 1, 1990
Molecular and cytogenetic analysis in two patients with microdeletions of 7p and Greig syndrome: hemizygosity for PGAM2 and TCRG genesK Wagner, P M Kroisel, W RosenkranzAmerican Journal of Medical Genetics|August 3, 2001
Phenotype of five patients with Greig syndrome and microdeletion of 7p13P M Kroisel, E Petek, K WagnerHuman Genetics|January 1, 1985
Simultaneous production of R-bands and either replication patterns or sister chromatid differentiationP M Kroisel, W Rosenkranz, D SchweizerGenetic Counseling (Geneva, Switzerland)|May 23, 2002
Mild phenotype due to inverse duplication 4p16.3 - P15.3 including the Wolf-Hirschhorn critical regionM Tschernigg, E Petek, K Wagner, et al.Cytogenetic and Genome Research|November 20, 2002
Chromosomal localization and genomic organization of the human Linker for Activation of T cells (LAT) geneC Windpassinger, P M Kroisel, K Wagner, et al.Cytogenetics and Cell Genetics|January 1, 1994
PCR probes for chromosome in situ hybridization of large-insert bacterial recombinantsP M Kroisel, P A Ioannou, P J de JongPageof 4