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HGG Advances|October 24, 2022
Large 22q13.3 deletions perturb peripheral transcriptomic and metabolomic profiles in Phelan-McDermid syndromeMichael S Breen, Xuanjia Fan, Tess Levy, et al.
Molecular Syndromology|November 1, 2012
Investigation of TBR1 Hemizygosity: Four Individuals with 2q24 MicrodeletionsR N Traylor, W B Dobyns, J A Rosenfeld, et al.
Cancer Research|September 29, 1998
Identification of germ-line E-cadherin mutations in gastric cancer families of European originS A Gayther, K L Gorringe, S J Ramus, et al.
Journal of the International Association of Providers of AIDS Care|November 13, 2025
Opportunities and Constraints to Equitable Implementation of the Revised Infant Feeding Guidelines for Pregnant and Lactating Persons Living With HIV in the United States: A Qualitative StudyAudrey J Buckland, Helen Schmedtje, Abinethaa Paramasivam, et al.
Pediatric Neurology|February 29, 2020
Diffusion Tensor Imaging Abnormalities in the Uncinate Fasciculus and Inferior Longitudinal Fasciculus in Phelan-McDermid SyndromeJulia Bassell, Siddharth Srivastava, Anna K Prohl, et al.
Scientific Data|November 28, 2023
A proteomic meta-analysis refinement of plasma extracellular vesiclesMilene C Vallejo, Soumyadeep Sarkar, Emily C Elliott, et al.
The Journal of Allergy and Clinical Immunology|April 16, 2008
The soluble form of a disintegrin and metalloprotease 33 promotes angiogenesis: implications for airway remodeling in asthmaIlaria Puxeddu, Yun Yun Pang, Anna Harvey, et al.
Human Mutation|August 31, 2006
Somatic mutations of GUCY2F, EPHA3, and NTRK3 in human cancersLaura D Wood, Eric S Calhoun, Natalie Silliman, et al.
Cold Spring Harbor Molecular Case Studies|April 28, 2022
Tuberous sclerosis complex: a complex caseRyan M Powell, Sharon Pattison, Jiri C Moravec, et al.
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