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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 56a
F H Herrmann, K Wulff, M Schütz, et al.
Padiatrie Und Grenzgebiete
|
January 1, 1982
[Tryptophan metabolism in infants with phenylketonuria]
P Bührdel, U Grimm, S Wässer, et al.
Journal of Neurology
|
December 1, 1989
Deletion screening in patients with Duchenne muscular dystrophy
K Wulff, F H Herrmann, M C Wapenaar, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
August 13, 2014
Characterization of a partial exon 9/intron 9 deletion in the coagulation factor XII gene (F12) detected in two Turkish families with hereditary angioedema and normal C1 inhibitor
K Bork, K Wulff, J Hardt, 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-penicillamine
J J Corrigan, M L Damiano, C Leissinger, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
November 24, 2016
Tamoxifen may cause life-threatening angioedema attacks in patients with hereditary angioedema
K Bork, K Wulff, G Witzke, et al.
Clinical Chemistry
|
August 1, 1985
Specific immunoassay of alpha-amylase isoenzymes in human serum
M 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 dystrophy
K 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 hospitals
L Solomon, C Thompson, L Squiers, et al.
Page
of 12
Search research articles
Search
Showing results (71-80 of 118) with videos related to
Sort By:
Page
of 12
European Journal of Pediatrics
|
January 1, 1990
Deletion screening and prenatal diagnosis of Duchenne muscular dystrophy using cDNA probes Cf 23a and Cf 56a
F H Herrmann, K Wulff, M Schütz, et al.
Padiatrie Und Grenzgebiete
|
January 1, 1982
[Tryptophan metabolism in infants with phenylketonuria]
P Bührdel, U Grimm, S Wässer, et al.
Journal of Neurology
|
December 1, 1989
Deletion screening in patients with Duchenne muscular dystrophy
K Wulff, F H Herrmann, M C Wapenaar, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
August 13, 2014
Characterization of a partial exon 9/intron 9 deletion in the coagulation factor XII gene (F12) detected in two Turkish families with hereditary angioedema and normal C1 inhibitor
K Bork, K Wulff, J Hardt, 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-penicillamine
J J Corrigan, M L Damiano, C Leissinger, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
November 24, 2016
Tamoxifen may cause life-threatening angioedema attacks in patients with hereditary angioedema
K Bork, K Wulff, G Witzke, et al.
Clinical Chemistry
|
August 1, 1985
Specific immunoassay of alpha-amylase isoenzymes in human serum
M 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 dystrophy
K 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 hospitals
L Solomon, C Thompson, L Squiers, et al.
Page
of 12