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Clinical Genetics|May 1, 1993
Chromosome painting using FISH (fluorescence in situ hybridization) with chromosome-6-specific library demonstrates the origin of a de novo 6q+ marker chromosomeK Brøndum-Nielsen, S Bajalica, K Wulff, et al.Acta Medica Scandinavica|January 1, 1980
Hydralazine in arterial hypertension. Randomized double-blind comparison of conventional/Slow-Release formulation and of b.i.d./q.i.d. dosage regimensK Wulff, K Lenz, A R Krogsgaard, et al.Thrombosis and Haemostasis|January 4, 1998
Haemophilia B in female twins caused by a point mutation in one factor IX gene and nonrandom inactivation patterns of the X-chromosomesW Schröder, K Wulff, K Wollina, et al.European Journal of Pediatrics|January 1, 1990
Deletion screening and prenatal diagnosis of Duchenne muscular dystrophy using cDNA probes Cf 23a and Cf 56aF H Herrmann, K Wulff, M Schütz, et al.Journal of Neurology|December 1, 1989
Deletion screening in patients with Duchenne muscular dystrophyK Wulff, F H Herrmann, M C Wapenaar, et al.Zeitschrift Fur Urologie Und Nephrologie|May 1, 1988
[Studies on tryptophan metabolism in calcium oxalate urolithiasis]U Grimm, I Steinhauser, K Wulff, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|February 1, 2003
Treatment of chronic haemophilic synovitis in humans with D-penicillamineJ J Corrigan, M L Damiano, C Leissinger, et al.Clinical Chemistry|August 1, 1985
Specific immunoassay of alpha-amylase isoenzymes in human serumM Gerber, K Naujoks, H Lenz, et al.Human Mutation|January 1, 1997
Six novel mutations in the emerin gene causing X-linked Emery-Dreifuss muscular dystrophyK Wulff, J E Parrish, F H Herrmann, et al.Infection Control and Hospital Epidemiology|July 8, 1999
Occupational exposure and voluntary human immunodeficiency virus testing: a survey of Maryland hospitalsL Solomon, C Thompson, L Squiers, et al.Pageof 11