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Nucleic Acids Research
|
April 25, 1991
Haemophilia B: database of point mutations and short additions and deletions--second edition
F Giannelli, P M Green, K A High, et al.
Surgical Innovation
|
November 1, 2013
Development and clinical implementation of a hemostatic balloon device for rectal cancer surgery
Fabian A Holman, Noortje van der Pant, Ignace H J T de Hingh, et al.
The Journal of Hospital Infection
|
May 16, 2022
Impact of sink design on bacterial transmission from hospital sink drains to the surrounding sink environment tested using a fluorescent marker
J Pirzadian, T Souhoka, M Herweijer, et al.
European Journal of Human Genetics : EJHG
|
May 1, 1997
CFTR gene mutations in adults with disseminated bronchiectasis
E Girodon, C Cazeneuve, F Lebargy, et al.
Blood
|
August 1, 1988
Hairy cell leukemia associated with large granular lymphocyte leukemia: immunologic and genomic study, effect of interferon treatment
J P Marolleau, T Henni, P Gaulard, et al.
Nouvelle Revue Francaise D'Hematologie
|
January 1, 1990
Expression of the alpha beta and gamma delta T-cell receptors in peripheral T-cell lymphomas
P Gaulard, P Bourquelot, P Kanavaros, et al.
Human Genetics
|
April 1, 1993
Nucleotide substitutions at the -6 position in the promoter region of the factor IX gene result in different severity of hemophilia B Leyden: consequences for genetic counseling
D Vidaud, M Tartary, J M Costa, et al.
International Journal of Environmental Research and Public Health
|
December 22, 2018
Healthy Nutrition and Physical Activity in Childcare: Views from Childcare Managers, Childcare Workers and Parents on Influential Factors
Ilona van de Kolk, Anne J M Goossens, Sanne M P L Gerards, et al.
Journal of Clinical Pathology
|
December 24, 2008
Neonatal screening for sickle cell disease in France
J Bardakdjian-Michau, M Bahuau, D Hurtrel, et al.
Human Molecular Genetics
|
August 11, 1999
A molecular analysis of the yemenite deaf-blind hypopigmentation syndrome: SOX10 dysfunction causes different neurocristopathies
N Bondurand, K Kuhlbrodt, V Pingault, et al.
Page
of 37
Search research articles
Search
Showing results (311-320 of 364) with videos related to
Sort By:
Page
of 37
Nucleic Acids Research
|
April 25, 1991
Haemophilia B: database of point mutations and short additions and deletions--second edition
F Giannelli, P M Green, K A High, et al.
Surgical Innovation
|
November 1, 2013
Development and clinical implementation of a hemostatic balloon device for rectal cancer surgery
Fabian A Holman, Noortje van der Pant, Ignace H J T de Hingh, et al.
The Journal of Hospital Infection
|
May 16, 2022
Impact of sink design on bacterial transmission from hospital sink drains to the surrounding sink environment tested using a fluorescent marker
J Pirzadian, T Souhoka, M Herweijer, et al.
European Journal of Human Genetics : EJHG
|
May 1, 1997
CFTR gene mutations in adults with disseminated bronchiectasis
E Girodon, C Cazeneuve, F Lebargy, et al.
Blood
|
August 1, 1988
Hairy cell leukemia associated with large granular lymphocyte leukemia: immunologic and genomic study, effect of interferon treatment
J P Marolleau, T Henni, P Gaulard, et al.
Nouvelle Revue Francaise D'Hematologie
|
January 1, 1990
Expression of the alpha beta and gamma delta T-cell receptors in peripheral T-cell lymphomas
P Gaulard, P Bourquelot, P Kanavaros, et al.
Human Genetics
|
April 1, 1993
Nucleotide substitutions at the -6 position in the promoter region of the factor IX gene result in different severity of hemophilia B Leyden: consequences for genetic counseling
D Vidaud, M Tartary, J M Costa, et al.
International Journal of Environmental Research and Public Health
|
December 22, 2018
Healthy Nutrition and Physical Activity in Childcare: Views from Childcare Managers, Childcare Workers and Parents on Influential Factors
Ilona van de Kolk, Anne J M Goossens, Sanne M P L Gerards, et al.
Journal of Clinical Pathology
|
December 24, 2008
Neonatal screening for sickle cell disease in France
J Bardakdjian-Michau, M Bahuau, D Hurtrel, et al.
Human Molecular Genetics
|
August 11, 1999
A molecular analysis of the yemenite deaf-blind hypopigmentation syndrome: SOX10 dysfunction causes different neurocristopathies
N Bondurand, K Kuhlbrodt, V Pingault, et al.
Page
of 37