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Nature Communications
|
August 2, 2020
A neurovascular high-frequency optical coherence tomography system enables in situ cerebrovascular volumetric microscopy
Giovanni J Ughi, Miklos G Marosfoi, Robert M King, et al.
American Journal of Medical Genetics. Part A
|
June 15, 2011
Phenotypic variability of distal 22q11.2 copy number abnormalities
Tiong Yang Tan, Amanda Collins, Paul A James, et al.
American Journal of Human Genetics
|
May 27, 2005
3q29 microdeletion syndrome: clinical and molecular characterization of a new syndrome
Lionel Willatt, James Cox, John Barber, et al.
Annals of Neurology
|
February 26, 2005
Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander disease
Rong Li, Anne B Johnson, Gajja Salomons, et al.
Early Intervention in Psychiatry
|
May 13, 2016
Secondary school teachers and mental health competence: Italy-United Kingdom comparison
Elena Monducci, Claudia Battaglia, Alberto Forte, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
October 13, 2020
Intratumoral Injection of <i>Clostridium novyi</i>-NT Spores in Patients with Treatment-refractory Advanced Solid Tumors
Filip Janku, Halle Huihong Zhang, Abdulmohammad Pezeshki, et al.
Science Translational Medicine
|
August 15, 2014
Intratumoral injection of Clostridium novyi-NT spores induces antitumor responses
Nicholas J Roberts, Linping Zhang, Filip Janku, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 17, 2004
Comparative PRKAR1A genotype-phenotype analyses in humans with Carney complex and prkar1a haploinsufficient mice
Mark Veugelers, David Wilkes, Kimberly Burton, et al.
The New England Journal of Medicine
|
September 12, 2008
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes
Heather C Mefford, Andrew J Sharp, Carl Baker, et al.
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of 3
Search research articles
Search
Showing results (21-30 of 29) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 29 results.
Nature Communications
|
August 2, 2020
A neurovascular high-frequency optical coherence tomography system enables in situ cerebrovascular volumetric microscopy
Giovanni J Ughi, Miklos G Marosfoi, Robert M King, et al.
American Journal of Medical Genetics. Part A
|
June 15, 2011
Phenotypic variability of distal 22q11.2 copy number abnormalities
Tiong Yang Tan, Amanda Collins, Paul A James, et al.
American Journal of Human Genetics
|
May 27, 2005
3q29 microdeletion syndrome: clinical and molecular characterization of a new syndrome
Lionel Willatt, James Cox, John Barber, et al.
Annals of Neurology
|
February 26, 2005
Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander disease
Rong Li, Anne B Johnson, Gajja Salomons, et al.
Early Intervention in Psychiatry
|
May 13, 2016
Secondary school teachers and mental health competence: Italy-United Kingdom comparison
Elena Monducci, Claudia Battaglia, Alberto Forte, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
October 13, 2020
Intratumoral Injection of <i>Clostridium novyi</i>-NT Spores in Patients with Treatment-refractory Advanced Solid Tumors
Filip Janku, Halle Huihong Zhang, Abdulmohammad Pezeshki, et al.
Science Translational Medicine
|
August 15, 2014
Intratumoral injection of Clostridium novyi-NT spores induces antitumor responses
Nicholas J Roberts, Linping Zhang, Filip Janku, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 17, 2004
Comparative PRKAR1A genotype-phenotype analyses in humans with Carney complex and prkar1a haploinsufficient mice
Mark Veugelers, David Wilkes, Kimberly Burton, et al.
The New England Journal of Medicine
|
September 12, 2008
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes
Heather C Mefford, Andrew J Sharp, Carl Baker, et al.
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of 3