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Human Mutation
|
January 1, 1992
Two novel mutations responsible for hereditary type I protein C deficiency: characterization by denaturing gradient gel electrophoresis
S Gandrille, M Vidaud, M Aiach, et al.
The British Journal of Surgery
|
June 3, 2011
Operative notes do not reflect reality in laparoscopic cholecystectomy
L S G L Wauben, W M U van Grevenstein, R H M Goossens, et al.
ACS Applied Materials & Interfaces
|
January 20, 2021
Scalable PbS Quantum Dot Solar Cell Production by Blade Coating from Stable Inks
Nataliia Sukharevska, Dmytro Bederak, Vincent M Goossens, et al.
The Open Orthopaedics Journal
|
April 3, 2010
Measurements of the exerted pressure by pelvic circumferential compression devices
Simon P Knops, Marcel P J M van Riel, Richard H M Goossens, et al.
Blood
|
January 1, 1994
Thrombocytopenia after bone marrow transplantation caused by a recipient origin Br(a) allo-antibody: presence of mixed chimerism 3 years after the graft without hematologic relapse
P Bierling, J M Pignon, M Kuentz, et al.
Nouvelle Revue Francaise D'Hematologie
|
January 1, 1989
The usefulness of phenotypic and genotypic studies in malignant lymphoma and related disorders
T Henni, P Gaulard, M Divine, et al.
Journal of Clinical Immunology
|
September 1, 1990
Polymerase chain reaction (PCR) amplification demonstrates the absence of human T-cell lymphotrophic virus (HTLV)-I specific pol sequences in peripheral T-cell lymphomas
T Henni, M Divine, P Gaulard, et al.
Journal of Materials Science. Materials in Medicine
|
August 10, 2006
Artificial midline-fascia of the human abdominal wall for testing suture strength
J M van Os, J F Lange, R H M Goossens, et al.
Human Genetics
|
January 1, 1996
A novel mutation in exon 17 of the beta-subunit of rod phosphodiesterase in two RP sisters of a consanguineous family
D Valverde, T Solans, D Grinberg, et al.
Metabolism: Clinical and Experimental
|
December 1, 1996
Severe resistance to insulin and insulin-like growth factor-I in cells from a patient with leprechaunism as a result of two mutations in the tyrosine kinase domain of the insulin receptor
C Desbois-Mouthon, C Danan, S Amselem, et al.
Page
of 37
Search research articles
Search
Showing results (291-300 of 364) with videos related to
Sort By:
Page
of 37
Human Mutation
|
January 1, 1992
Two novel mutations responsible for hereditary type I protein C deficiency: characterization by denaturing gradient gel electrophoresis
S Gandrille, M Vidaud, M Aiach, et al.
The British Journal of Surgery
|
June 3, 2011
Operative notes do not reflect reality in laparoscopic cholecystectomy
L S G L Wauben, W M U van Grevenstein, R H M Goossens, et al.
ACS Applied Materials & Interfaces
|
January 20, 2021
Scalable PbS Quantum Dot Solar Cell Production by Blade Coating from Stable Inks
Nataliia Sukharevska, Dmytro Bederak, Vincent M Goossens, et al.
The Open Orthopaedics Journal
|
April 3, 2010
Measurements of the exerted pressure by pelvic circumferential compression devices
Simon P Knops, Marcel P J M van Riel, Richard H M Goossens, et al.
Blood
|
January 1, 1994
Thrombocytopenia after bone marrow transplantation caused by a recipient origin Br(a) allo-antibody: presence of mixed chimerism 3 years after the graft without hematologic relapse
P Bierling, J M Pignon, M Kuentz, et al.
Nouvelle Revue Francaise D'Hematologie
|
January 1, 1989
The usefulness of phenotypic and genotypic studies in malignant lymphoma and related disorders
T Henni, P Gaulard, M Divine, et al.
Journal of Clinical Immunology
|
September 1, 1990
Polymerase chain reaction (PCR) amplification demonstrates the absence of human T-cell lymphotrophic virus (HTLV)-I specific pol sequences in peripheral T-cell lymphomas
T Henni, M Divine, P Gaulard, et al.
Journal of Materials Science. Materials in Medicine
|
August 10, 2006
Artificial midline-fascia of the human abdominal wall for testing suture strength
J M van Os, J F Lange, R H M Goossens, et al.
Human Genetics
|
January 1, 1996
A novel mutation in exon 17 of the beta-subunit of rod phosphodiesterase in two RP sisters of a consanguineous family
D Valverde, T Solans, D Grinberg, et al.
Metabolism: Clinical and Experimental
|
December 1, 1996
Severe resistance to insulin and insulin-like growth factor-I in cells from a patient with leprechaunism as a result of two mutations in the tyrosine kinase domain of the insulin receptor
C Desbois-Mouthon, C Danan, S Amselem, et al.
Page
of 37