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Human Molecular Genetics|January 1, 1994
Frequency of common and novel inactivating APC mutations in 202 families with familial adenomatous polyposisM Mandl, R Paffenholz, W Friedl, et al.Human Genetics|April 1, 1989
Pseudodeficiency of arylsulfatase A: a common genetic polymorphism with possible disease implicationsC Hohenschutz, P Eich, W Friedl, et al.Brain Research|April 19, 1988
The shark GABA-benzodiazepine receptor: further evidence for a not so late phylogenetic appearance of the benzodiazepine receptorJ Hebebrand, W Friedl, R Reichelt, et al.Psychiatria Clinica|January 1, 1983
Dexamethasone suppression test combined with total sleep deprivation in depressed patientsS Kasper, H W Moises, H BeckmannPharmacopsychiatria|September 1, 1981
Trazodone and amitriptyline in treatment of depressed inpatients. A double-blind studyH W Moises, S Kasper, H BeckmannPharmacopsychiatria|November 1, 1981
The anticholinergic biperiden in depressive disordersS Kasper, H W Moises, H BeckmannHuman Heredity|April 4, 1998
A novel missense mutation in the DNA mismatch repair gene hMLH1 present among East Asians but not among EuropeansY Wang, W Friedl, C Lamberti, et al.Human Genetics|May 1, 1996
Attenuated familial adenomatous polyposis due to a mutation in the 3' part of the APC gene. A clue for understanding the function of the APC proteinW Friedl, S Meuschel, R Caspari, et al.Archiv Fur Psychiatrie Und Nervenkrankheiten|January 1, 1983
Phenylethylamine and phenylacetic acid in CSF of schizophrenics and healthy controlsH Beckmann, G P Reynolds, M Sandler, et al.Cancer Detection and Prevention|March 29, 2001
Detection of APC and k-ras mutations in the serum of patients with colorectal cancerH Lauschke, R Caspari, W Friedl, et al.Pageof 103