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Journal of Neural Transmission (Vienna, Austria : 1996)|March 27, 2003
The future of genetic association studies in Alzheimer diseaseU FinckhBiotechniques|January 1, 1991
Producing single-stranded DNA probes with the Taq DNA polymerase: a high yield protocolU Finckh, P A Lingenfelter, D MyersonClinical and Experimental Dermatology|January 1, 1996
Absence of human T-lymphotrophic virus type I in patients with systemic lupus erythematosusK Lipka, B Tebbe, U Finckh, et al.Obesity Reviews : an Official Journal of the International Association for the Study of Obesity|October 23, 2009
Variegate porphyria in a 46-year-old patient taking sibutramine for weight lossM Reiser, S Eickmann, T Haverkamp, et al.HNO|February 24, 2001
[Congenital hearing disorders in children. 1: Acquired hearing disorders]M Gross, U Finckh-Krämer, M Spormann-LagodzinskiInternational Journal of Pediatric Otorhinolaryngology|December 15, 2000
German registry for hearing loss in children: results after 4 yearsU Finckh-Krämer, M Spormann-Lagodzinski, M GrossHNO|April 26, 2001
[Siblings with pediatric hearing loss. Data on age at diagnosis and degree of hearing loss]U Finckh-Krämer, M E Spormann-Lagodzinski, M GrossHNO|June 2, 1998
[Data protection for the national German Central Registry of Pediatric Hearing Disorders]U Finckh-Krämer, M Hess, M Gross, et al.DNA Sequence : the Journal of DNA Sequencing and Mapping|January 1, 1996
Allele-specific PCR for simultaneous amplification of both alleles of a deletion polymorphism in intron 6 of the human dopamine 2 receptor gene (DRD2)U Finckh, H Rommelspacher, L G Schmidt, et al.American Journal of Medical Genetics|May 8, 2000
Spectrum and detection rate of L1CAM mutations in isolated and familial cases with clinically suspected L1-diseaseU Finckh, J Schröder, B Ressler, et al.Pageof 5