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Circulation|December 28, 2006
Mutations in the gene encoding filamin A as a cause for familial cardiac valvular dystrophyFlorence Kyndt, Jean-Pierre Gueffet, Vincent Probst, et al.Open Heart|February 21, 2020
Association between hypertension and retinal vascular features in ultra-widefield fundus imagingGavin Robertson, Alan Fleming, Michelle Claire Williams, et al.Advanced Materials (Deerfield Beach, Fla.)|May 30, 2020
Ultralow Voltage Manipulation of FerromagnetismBhagwati Prasad, Yen-Lin Huang, Rajesh V Chopdekar, et al.American Journal of Human Genetics|May 31, 2003
Ehlers-Danlos syndrome with severe early-onset periodontal disease (EDS-VIII) is a distinct, heterogeneous disorder with one predisposition gene at chromosome 12p13Nazneen Rahman, Melanie Dunstan, M Dawn Teare, et al.Nature Communications|March 3, 2022
The role of lattice dynamics in ferroelectric switchingQiwu Shi, Eric Parsonnet, Xiaoxing Cheng, et al.European Journal of Nutrition|July 20, 2019
Iodine status of teenage girls on the island of IrelandKaren Mullan, Lesley Hamill, Katy Doolan, et al.Nature Communications|June 7, 2020
Manipulating magnetoelectric energy landscape in multiferroicsYen-Lin Huang, Dmitri Nikonov, Christopher Addiego, et al.Nature Communications|April 17, 2025
Room-temperature multiferroicity in sliding van der Waals semiconductors with sub-0.3 V switchingRui Chen, Fanhao Meng, Hongrui Zhang, et al.American Journal of Human Genetics|June 9, 2004
Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardationPatrick Tarpey, Josep Parnau, Matthew Blow, et al.Human Mutation|April 28, 2012
Further delineation of CANT1 phenotypic spectrum and demonstration of its role in proteoglycan synthesisMathilde Nizon, Céline Huber, Fabio De Leonardis, et al.Pageof 16