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BMC Bioinformatics|October 7, 2006
Coloring the Mu transpososomeIsabel K Darcy, Jeff Chang, Nathan Druivenga, et al.
Journal of Medical Genetics|April 14, 2012
Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphaloceleUppala Radhakrishna, Swapan K Nath, Ken McElreavey, et al.
Scientific Reports|December 24, 2025
Transcriptomic signatures in brain and blood related to cognitive and psychiatric phenotypes of Prader-Willi syndromeShokouh Shahrokhi, Emma K Baker, Michael See, et al.
The Journal of Clinical Endocrinology and Metabolism|January 13, 2023
Diazoxide Choline Extended-Release Tablet in People With Prader-Willi Syndrome: A Double-Blind, Placebo-Controlled TrialJennifer L Miller, Evelien Gevers, Nicola Bridges, et al.
ACS Omega|October 16, 2023
Polymeric Backbone Eutectogel Electrolytes for High-Energy Lithium-Ion BatteriesAn-Sofie Kelchtermans, Bjorn Joos, Dries De Sloovere, et al.
Physical Chemistry Chemical Physics : PCCP|May 17, 2014
Conversion efficiency of skutterudite-based thermoelectric modulesJames R Salvador, Jung Y Cho, Zuxin Ye, et al.
JAMA Network Open|January 4, 2022
Feasibility of Screening for Chromosome 15 Imprinting Disorders in 16 579 Newborns by Using a Novel Genomic WorkflowDavid E Godler, Ling Ling, Dinusha Gamage, et al.
Journal of Neurovirology|December 16, 2017
Symptomatic cerebrospinal fluid HIV-1 escape with no resistance-associated mutations following low-level plasma viremiaMattia Trunfio, Sarah Beth Joseph, Valeria Ghisetti, et al.
American Journal of Medical Genetics. Part A|November 15, 2007
Neuroimaging findings in macrocephaly-capillary malformation: a longitudinal study of 17 patientsRobert L Conway, Barry D Pressman, William B Dobyns, et al.
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