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Talbot

Showing results (1351-1360 of 6,399) with videos related to

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World Journal of Gastroenterology|May 24, 2006
Clinico-pathological aspects of colorectal serrated adenomasAshish Chandra, Adnan A Sheikh, Anton Cerar, et al.
JID Innovations : Skin Science From Molecules to Population Health|January 13, 2022
Presence of Uterine Leiomyomas Has No Significant Impact on Gene Expression Profile in the Scalp of Patients with Central Centrifugal Cicatricial AlopeciaTaylor A Jamerson, C Conover Talbot, Yemisi Dina, et al.
Science Advances|August 31, 2022
A lysosomal regulatory circuit essential for the development and function of microgliaHarini Iyer, Kimberle Shen, Ana M Meireles, et al.
Dementia (London, England)|March 26, 2021
The use of Twitter by people with young-onset dementia: A qualitative analysis of narratives and identity formation in the age of social mediaCatherine V Talbot, Siobhan T O'Dwyer, Linda Clare, et al.
Journal of Orthopaedic Trauma|June 24, 2011
Extra-articular malunions of the scapula: a comparison of functional outcome before and after reconstructionPeter A Cole, Max Talbot, Lisa K Schroder, et al.
IEEE Transactions on Pattern Analysis and Machine Intelligence|September 11, 2015
Directed Connected Operators: Asymmetric Hierarchies for Image Filtering and SegmentationBenjamin Perret, Jean Cousty, Olena Tankyevych, et al.
International Journal of Obesity|January 1, 1983
Association between serum high-density lipoprotein cholesterol and body composition in adult menS Leclerc, C Bouchard, J Talbot, et al.
The Journal of Family Practice|March 1, 1981
The telephone survey in family practiceP Curtis, A Talbot, S Evens, et al.
Differentiation; Research in Biological Diversity|June 1, 1993
Expression from the proximal promoter of the carbonic anhydrase 1 gene as a marker for differentiation in colon epitheliaJ Sowden, S Leigh, I Talbot, et al.
Journal of Medical Genetics|December 1, 1996
Evidence for compound heterozygosity causing mild and severe forms of autosomal recessive spinal muscular atrophyK Talbot, N Rodrigues, G Bernert, et al.
Pageof 640

Showing results (1351-1360 of 6,399) with videos related to

Sort By:
Pageof 640
World Journal of Gastroenterology|May 24, 2006
Clinico-pathological aspects of colorectal serrated adenomasAshish Chandra, Adnan A Sheikh, Anton Cerar, et al.
JID Innovations : Skin Science From Molecules to Population Health|January 13, 2022
Presence of Uterine Leiomyomas Has No Significant Impact on Gene Expression Profile in the Scalp of Patients with Central Centrifugal Cicatricial AlopeciaTaylor A Jamerson, C Conover Talbot, Yemisi Dina, et al.
Science Advances|August 31, 2022
A lysosomal regulatory circuit essential for the development and function of microgliaHarini Iyer, Kimberle Shen, Ana M Meireles, et al.
Dementia (London, England)|March 26, 2021
The use of Twitter by people with young-onset dementia: A qualitative analysis of narratives and identity formation in the age of social mediaCatherine V Talbot, Siobhan T O'Dwyer, Linda Clare, et al.
Journal of Orthopaedic Trauma|June 24, 2011
Extra-articular malunions of the scapula: a comparison of functional outcome before and after reconstructionPeter A Cole, Max Talbot, Lisa K Schroder, et al.
IEEE Transactions on Pattern Analysis and Machine Intelligence|September 11, 2015
Directed Connected Operators: Asymmetric Hierarchies for Image Filtering and SegmentationBenjamin Perret, Jean Cousty, Olena Tankyevych, et al.
International Journal of Obesity|January 1, 1983
Association between serum high-density lipoprotein cholesterol and body composition in adult menS Leclerc, C Bouchard, J Talbot, et al.
The Journal of Family Practice|March 1, 1981
The telephone survey in family practiceP Curtis, A Talbot, S Evens, et al.
Differentiation; Research in Biological Diversity|June 1, 1993
Expression from the proximal promoter of the carbonic anhydrase 1 gene as a marker for differentiation in colon epitheliaJ Sowden, S Leigh, I Talbot, et al.
Journal of Medical Genetics|December 1, 1996
Evidence for compound heterozygosity causing mild and severe forms of autosomal recessive spinal muscular atrophyK Talbot, N Rodrigues, G Bernert, et al.
Pageof 640