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Clinical Genetics|March 1, 1990
High resolution banding of an unusual reciprocal translocation in recurrent abortionsP M Kroisel, W RosenkranzJournal of Medical Genetics|March 10, 2009
Predictive diagnosis of the cancer prone Li-Fraumeni syndrome by accident: new challenges through whole genome array testingT Schwarzbraun, A C Obenauf, A Langmann, et al.Fortschritte Der Neurologie-Psychiatrie|November 5, 2005
[Genetic risk factors in schizophrenia]H Fabisch, P M Kroisel, Karin FabischHuman Genetics|January 1, 1985
Simultaneous production of R-bands and either replication patterns or sister chromatid differentiationP M Kroisel, W Rosenkranz, D SchweizerBrain : a Journal of Neurology|July 25, 2000
Phenotypic and genotypic heterogeneity in hereditary motor neuronopathy type V: a clinical, electrophysiological and genetic studyM Auer-Grumbach, W N Löscher, 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 JongAmerican Journal of Medical Genetics|November 15, 2000
Homozygosity for the W151X stop mutation in the delta7-sterol reductase gene (DHCR7) causing a lethal form of Smith-Lemli-Opitz syndrome: retrospective molecular diagnosisJ Löffler, A Trojovsky, B Casati, et al.Human Molecular Genetics|December 1, 1992
Microdissection of a human marker chromosome reveals its origin and a new family of centromeric repetitive DNAD H Johnson, P M Kroisel, H J Klapper, et al.Cancer|November 15, 1991
Acute megakaryocytic leukemia in children. Clinical, immunologic, and cytogenetic findings in two patientsI Slavc, C Urban, O A Haas, et al.Nature Genetics|March 10, 2001
Maternal methylation imprints on human chromosome 15 are established during or after fertilizationO El-Maarri, K Buiting, E G Peery, et al.Pageof 157