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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.Elife|September 9, 2016
Two locus inheritance of non-syndromic midline craniosynostosis via rare <i>SMAD6</i> and common <i>BMP2</i> allelesAndrew T Timberlake, Jungmin Choi, Samir Zaidi, 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.Nature Biotechnology|September 12, 2006
The MicroArray Quality Control (MAQC) project shows inter- and intraplatform reproducibility of gene expression measurements, Leming Shi, Laura H Reid, et al.Pageof 3