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Human Mutation
|
January 1, 1995
Twenty-five novel mutations of the factor IX gene in haemophilia B
K Wulff, W Schröder, M Wehnert, et al.
European Journal of Pediatrics
|
August 1, 1993
Molybdenum cofactor deficiency in two siblings: diagnostic difficulties
L K Hansen, K Wulff, C Dorche, et al.
Ugeskrift for Laeger
|
May 2, 1977
[Clinical--pharmacological aspects of treatment with sodium di-n-propylacetate]
K Wulff, H Flachs, A Würtz-Jørgensen, et al.
Ugeskrift for Laeger
|
September 5, 1994
[Early treatment with nasal continuous positive airway pressure and "minimal handling". Early and late prognosis in children with birth weight under 1,501 g]
J Kamper, K Wulff, C O Larsen, et al.
Journal of Refractive Surgery (Thorofare, N.J. : 1995)
|
April 15, 1999
Worst-Fechner biconcave minus power phakic iris-claw lens
P U Fechner, I Haubitz, W Wichmann, et al.
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 chromosome
K Brøndum-Nielsen, S Bajalica, K Wulff, et al.
Epilepsia
|
June 1, 1977
Clinical pharmacological aspects of valproate sodium
K Wulff, H Flachs, A Würtz-Jorgensen, 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 regimens
K 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-chromosomes
W Schröder, K Wulff, K Wollina, et al.
Ugeskrift for Laeger
|
July 14, 1980
[Hydralazine in arterial hypertension. Randomized, double-blind comparison between conventional and slow-release preparations]
K Wulff, K Lenz, A R Krogsgaard, et al.
Page
of 12
Search research articles
Search
Showing results (61-70 of 118) with videos related to
Sort By:
Page
of 12
Human Mutation
|
January 1, 1995
Twenty-five novel mutations of the factor IX gene in haemophilia B
K Wulff, W Schröder, M Wehnert, et al.
European Journal of Pediatrics
|
August 1, 1993
Molybdenum cofactor deficiency in two siblings: diagnostic difficulties
L K Hansen, K Wulff, C Dorche, et al.
Ugeskrift for Laeger
|
May 2, 1977
[Clinical--pharmacological aspects of treatment with sodium di-n-propylacetate]
K Wulff, H Flachs, A Würtz-Jørgensen, et al.
Ugeskrift for Laeger
|
September 5, 1994
[Early treatment with nasal continuous positive airway pressure and "minimal handling". Early and late prognosis in children with birth weight under 1,501 g]
J Kamper, K Wulff, C O Larsen, et al.
Journal of Refractive Surgery (Thorofare, N.J. : 1995)
|
April 15, 1999
Worst-Fechner biconcave minus power phakic iris-claw lens
P U Fechner, I Haubitz, W Wichmann, et al.
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 chromosome
K Brøndum-Nielsen, S Bajalica, K Wulff, et al.
Epilepsia
|
June 1, 1977
Clinical pharmacological aspects of valproate sodium
K Wulff, H Flachs, A Würtz-Jorgensen, 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 regimens
K 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-chromosomes
W Schröder, K Wulff, K Wollina, et al.
Ugeskrift for Laeger
|
July 14, 1980
[Hydralazine in arterial hypertension. Randomized, double-blind comparison between conventional and slow-release preparations]
K Wulff, K Lenz, A R Krogsgaard, et al.
Page
of 12