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Nature|June 24, 2016
A complement-microglial axis drives synapse loss during virus-induced memory impairmentMichael J Vasek, Charise Garber, Denise Dorsey, et al.
Human Genetics|December 12, 2018
De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairmentJeroen J Smits, Jaap Oostrik, Andy J Beynon, et al.
Plos Genetics|October 7, 2015
The Dynamic Genome and Transcriptome of the Human Fungal Pathogen Blastomyces and Close Relative EmmonsiaJosé F Muñoz, Gregory M Gauthier, Christopher A Desjardins, et al.
European Journal of Human Genetics : EJHG|November 3, 2016
Dominant variants in the splicing factor PUF60 cause a recognizable syndrome with intellectual disability, heart defects and short statureSalima El Chehadeh, Wilhelmina S Kerstjens-Frederikse, Julien Thevenon, et al.
European Journal of Endocrinology|August 10, 2022
Progressive diastolic dysfunction in survivors of pediatric differentiated thyroid carcinomaAntoinette D Reichert, Marloes Nies, Wim J E Tissing, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 29, 2016
Cardiovascular malformations caused by NOTCH1 mutations do not keep left: data on 428 probands with left-sided CHD and their familiesWilhelmina S Kerstjens-Frederikse, Ingrid M B H van de Laar, Yvonne J Vos, et al.
The Journal of Clinical Endocrinology and Metabolism|December 22, 2016
Long-Term Quality of Life in Adult Survivors of Pediatric Differentiated Thyroid CarcinomaMarloes Nies, Mariëlle S Klein Hesselink, Gea A Huizinga, et al.
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