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Human Genetics|February 1, 1990
Rapid detection of deletions in the Duchenne muscular dystrophy gene by PCR amplification of deletion-prone exon sequencesM Hentemann, J Reiss, M Wagner, et al.Molecular Biology & Medicine|August 1, 1990
Direct gene diagnosis of cystic fibrosis by allele-specific polymerase chain reactionsM Wagner, M Schloesser, J ReissOrganic Letters|May 24, 2000
Asymmetric epoxy cyclohexenyl sulfones: readily accessible progenitors of stereo defined six-carbon arraysM Hentemann, P L FuchsHuman Heredity|March 1, 1993
Allele frequencies of DNA markers genetically linked to Friedreich ataxia in the German populationC Zühlke, U ThiesDer Nervenarzt|January 1, 1996
[Huntington chorea. Molecular genetic principles, mutation detection and predictive diagnosis]C Zühlke, U ThiesZentralblatt Fur Neurochirurgie|January 1, 1983
[Postoperative treatment phases following the Cloward operation]D Pittasch, U ThiesEuropean Journal of Pediatrics|February 1, 1991
Prenatal deletion detection in a sporadic case of Duchenne muscular dystrophy without genotype information from the affected individualF Peinemann, M Wagner, U Franke, et al.Nucleic Acids Research|February 25, 1990
The effect of replication errors on the mismatch analysis of PCR-amplified DNAJ Reiss, M Krawczak, M Schloesser, et al.Journal of Medical Genetics|December 1, 1993
Attitudes of neurologists, psychiatrists, and psychotherapists towards predictive testing for Huntington's disease in GermanyU Thies, B Bockel, V BochdalofskyPrenatal Diagnosis|September 1, 1989
Abnormal pregnancy sonogram and chromosomal anomalies: four years' experience with rapid karyotypingM Hentemann, R Rauskolb, R Ulbrich, et al.Pageof 280