Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

J Clayton

Showing results (331-340 of 407) with videos related to

Pageof 41
Sort By:
Eye (London, England)|June 18, 2016
Diagnosing the cause of bilateral paediatric cataracts: comparison of standard testing with a next-generation sequencing approachM Musleh, G Hall, I C Lloyd, et al.
The Journal of Trauma and Acute Care Surgery|December 19, 2015
Dead or alive? New confirmatory test using quantitative analysis of computed tomographic angiographyLorena P Suarez-Kelly, Dhruv A Patel, Peter M Britt, et al.
Human Reproduction (Oxford, England)|December 20, 2005
Assisted reproductive therapies and imprinting disorders--a preliminary British surveyA G Sutcliffe, C J Peters, S Bowdin, et al.
European Journal of Medical Genetics|October 24, 2006
Tall stature and duplication of the insulin-like growth factor I receptor geneS G Kant, M Kriek, M J E Walenkamp, et al.
Structure (London, England : 1993)|December 3, 2014
Structural basis of receptor sulfotyrosine recognition by a CC chemokine: the N-terminal region of CCR3 bound to CCL11/eotaxin-1Christopher J Millard, Justin P Ludeman, Meritxell Canals, et al.
Clinical Dysmorphology|November 14, 1997
Macrocephaly with cutis marmorata, haemangioma and syndactyly--a distinctive overgrowth syndromeJ Clayton-Smith, B Kerr, H Brunner, et al.
Tissue Antigens|March 19, 1999
HLA-A, -B, -C polymorphism in a UK Ashkenazi Jewish potential bone marrow donor populationS T Cox, S G Marsh, I Scott, et al.
Journal of Medical Genetics|June 1, 1997
Large scale deletions in the GPC3 gene may account for a minority of cases of Simpson-Golabi-Behmel syndromeS Lindsay, M Ireland, O O'Brien, et al.
Journal of Alzheimer'S Disease : JAD|April 26, 2024
Real World Financial Mismanagement in Alzheimer's Disease, Frontotemporal Dementia, and Primary Progressive AphasiaSang Ngo, Ashley J Jackson, Madhumitha Manivannan, et al.
Clinical Chemistry|December 6, 2000
K-ras point mutation detection in lung cancer: comparison of two approaches to somatic mutation detection using ARMS allele-specific amplificationS J Clayton, F M Scott, J Walker, et al.
Pageof 41

Showing results (331-340 of 407) with videos related to

Sort By:
Pageof 41
Eye (London, England)|June 18, 2016
Diagnosing the cause of bilateral paediatric cataracts: comparison of standard testing with a next-generation sequencing approachM Musleh, G Hall, I C Lloyd, et al.
The Journal of Trauma and Acute Care Surgery|December 19, 2015
Dead or alive? New confirmatory test using quantitative analysis of computed tomographic angiographyLorena P Suarez-Kelly, Dhruv A Patel, Peter M Britt, et al.
Human Reproduction (Oxford, England)|December 20, 2005
Assisted reproductive therapies and imprinting disorders--a preliminary British surveyA G Sutcliffe, C J Peters, S Bowdin, et al.
European Journal of Medical Genetics|October 24, 2006
Tall stature and duplication of the insulin-like growth factor I receptor geneS G Kant, M Kriek, M J E Walenkamp, et al.
Structure (London, England : 1993)|December 3, 2014
Structural basis of receptor sulfotyrosine recognition by a CC chemokine: the N-terminal region of CCR3 bound to CCL11/eotaxin-1Christopher J Millard, Justin P Ludeman, Meritxell Canals, et al.
Clinical Dysmorphology|November 14, 1997
Macrocephaly with cutis marmorata, haemangioma and syndactyly--a distinctive overgrowth syndromeJ Clayton-Smith, B Kerr, H Brunner, et al.
Tissue Antigens|March 19, 1999
HLA-A, -B, -C polymorphism in a UK Ashkenazi Jewish potential bone marrow donor populationS T Cox, S G Marsh, I Scott, et al.
Journal of Medical Genetics|June 1, 1997
Large scale deletions in the GPC3 gene may account for a minority of cases of Simpson-Golabi-Behmel syndromeS Lindsay, M Ireland, O O'Brien, et al.
Journal of Alzheimer'S Disease : JAD|April 26, 2024
Real World Financial Mismanagement in Alzheimer's Disease, Frontotemporal Dementia, and Primary Progressive AphasiaSang Ngo, Ashley J Jackson, Madhumitha Manivannan, et al.
Clinical Chemistry|December 6, 2000
K-ras point mutation detection in lung cancer: comparison of two approaches to somatic mutation detection using ARMS allele-specific amplificationS J Clayton, F M Scott, J Walker, et al.
Pageof 41