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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.
Diagnostic Microbiology and Infectious Disease|November 11, 1991
Specimen cross-contamination by a strain of Mycobacterium tuberculosis lacking nitrate reductase activityW B Smith, D W Vance
Archives of Neurology|September 1, 1979
Micromyoclonic seizures of sleepP R Ash, W B Smith
The American Journal of Hospice & Palliative Care|February 8, 2000
Family surveys: measuring more than just satisfactionT A Welk, W B Smith
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