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Faraday Discussions
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February 17, 2011
Copper dioxygen (bio)inorganic chemistry
Edward I Solomon, Jake W Ginsbach, David E Heppner, et al.
Cellular Oncology : the Official Journal of the International Society for Cellular Oncology
|
July 28, 2009
Genetic classification of oral and oropharyngeal carcinomas identifies subgroups with a different prognosis
Serge J Smeets, Ruud H Brakenhoff, Bauke Ylstra, et al.
Genetic Counseling (Geneva, Switzerland)
|
November 4, 2004
Hypotriploidy 68,XX: a new case report and review of earlier cases
Y M Hoedemaekers, M J K De Kleine, M J P L Stevens-Kroef, et al.
Molecular Human Reproduction
|
October 23, 1998
Preimplantation genetic diagnosis of spinal muscular atrophy
J C Dreesen, M Bras, C de Die-Smulders, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
January 27, 2019
Hypercholesterolemia Induces a Mast Cell-CD4<sup>+</sup> T Cell Interaction in Atherosclerosis
Eva Kritikou, Thomas van der Heijden, Maarten Swart, et al.
Internet Interventions
|
December 5, 2018
Process evaluation of a social support platform 'Inlife' for caregivers of people with dementia
Alieske E H Dam, Hannah L Christie, Claudia M J Smeets, et al.
Genetic Counseling (Geneva, Switzerland)
|
July 28, 1999
Duplication within chromosome region 15q11-q13 in a patient with similarities to Prader-Willi syndrome confirmed by region-specific and band-specific fish
J J Engelen, W J Loots, J C Albrechts, et al.
Journal of Vascular and Interventional Radiology : JVIR
|
February 26, 2008
Long-term outcome of uterine artery embolization for symptomatic uterine leiomyomas
Paul N M Lohle, Marianne J Voogt, Jolanda De Vries, et al.
American Journal of Ophthalmology
|
March 28, 2006
Influence of mutation type on clinical expression of Leber hereditary optic neuropathy
Liesbeth Spruijt, Dinanda N Kolbach, Rene F de Coo, et al.
Annals of Neurology
|
January 23, 1999
A 4-base pair deletion in the mitochondrial cytochrome b gene associated with parkinsonism/MELAS overlap syndrome
I F De Coo, W O Renier, W Ruitenbeek, et al.
Page
of 71
Search research articles
Search
Showing results (531-540 of 709) with videos related to
Sort By:
Page
of 71
Faraday Discussions
|
February 17, 2011
Copper dioxygen (bio)inorganic chemistry
Edward I Solomon, Jake W Ginsbach, David E Heppner, et al.
Cellular Oncology : the Official Journal of the International Society for Cellular Oncology
|
July 28, 2009
Genetic classification of oral and oropharyngeal carcinomas identifies subgroups with a different prognosis
Serge J Smeets, Ruud H Brakenhoff, Bauke Ylstra, et al.
Genetic Counseling (Geneva, Switzerland)
|
November 4, 2004
Hypotriploidy 68,XX: a new case report and review of earlier cases
Y M Hoedemaekers, M J K De Kleine, M J P L Stevens-Kroef, et al.
Molecular Human Reproduction
|
October 23, 1998
Preimplantation genetic diagnosis of spinal muscular atrophy
J C Dreesen, M Bras, C de Die-Smulders, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
January 27, 2019
Hypercholesterolemia Induces a Mast Cell-CD4<sup>+</sup> T Cell Interaction in Atherosclerosis
Eva Kritikou, Thomas van der Heijden, Maarten Swart, et al.
Internet Interventions
|
December 5, 2018
Process evaluation of a social support platform 'Inlife' for caregivers of people with dementia
Alieske E H Dam, Hannah L Christie, Claudia M J Smeets, et al.
Genetic Counseling (Geneva, Switzerland)
|
July 28, 1999
Duplication within chromosome region 15q11-q13 in a patient with similarities to Prader-Willi syndrome confirmed by region-specific and band-specific fish
J J Engelen, W J Loots, J C Albrechts, et al.
Journal of Vascular and Interventional Radiology : JVIR
|
February 26, 2008
Long-term outcome of uterine artery embolization for symptomatic uterine leiomyomas
Paul N M Lohle, Marianne J Voogt, Jolanda De Vries, et al.
American Journal of Ophthalmology
|
March 28, 2006
Influence of mutation type on clinical expression of Leber hereditary optic neuropathy
Liesbeth Spruijt, Dinanda N Kolbach, Rene F de Coo, et al.
Annals of Neurology
|
January 23, 1999
A 4-base pair deletion in the mitochondrial cytochrome b gene associated with parkinsonism/MELAS overlap syndrome
I F De Coo, W O Renier, W Ruitenbeek, et al.
Page
of 71