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Medrxiv : the Preprint Server for Health Sciences|June 12, 2026
Quantifying donor-recipient mismatches using recipient-derived sources of donor DNANallakkandi Rajeevan, Gabriel C Barsotti, Ashwani Kumar, et al.
Annals of Neurology|September 1, 2017
GABBR2 mutations determine phenotype in rett syndrome and epileptic encephalopathyYongjin Yoo, Jane Jung, Yoo-Na Lee, et al.
Science (New York, N.Y.)|January 20, 2016
De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomaliesJason Homsy, Samir Zaidi, Yufeng Shen, et al.
Journal of Neurosurgery|October 27, 2019
Correlations between genomic subgroup and clinical features in a cohort of more than 3000 meningiomasMark W Youngblood, Daniel Duran, Julio D Montejo, et al.
Science Translational Medicine|February 15, 2023
Age-dependent impairment in antibody responses elicited by a homologous CoronaVac booster doseBruno Andraus Filardi, Valter Silva Monteiro, Pedro Vellosa Schwartzmann, et al.
Nature Genetics|March 15, 2011
Genome-wide association study identifies susceptibility loci for IgA nephropathyAli G Gharavi, Krzysztof Kiryluk, Murim Choi, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 24, 2025
Genomic analysis of 11,555 probands identifies 60 dominant congenital heart disease genesMichael C Sierant, Sheng Chih Jin, Kaya Bilguvar, et al.
Neuron|July 10, 2018
De Novo Mutation in Genes Regulating Neural Stem Cell Fate in Human Congenital HydrocephalusCharuta Gavankar Furey, Jungmin Choi, Sheng Chih Jin, et al.
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