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Plos One|September 21, 2017
Biometric and structural ocular manifestations of Marfan syndromePetra Gehle, Barbara Goergen, Daniel Pilger, et al.The Turkish Journal of Pediatrics|June 28, 2012
Arterial tortuosity and aneurysm in a case of Loeys-Dietz syndrome type IB with a mutation p.R537P in the TGFBR2 geneEsra Kiliç, Yasemin Alanay, Eda Utine, et al.Genome Research|July 12, 2015
Saturation analysis of ChIP-seq data for reproducible identification of binding peaksPeter Hansen, Jochen Hecht, Daniel M Ibrahim, et al.Genome Medicine|December 15, 2016
Alternate-locus aware variant calling in whole genome sequencingMarten Jäger, Max Schubach, Tomasz Zemojtel, et al.Journal of Medical Systems|October 23, 2012
Summarizing phenotype evolution patterns from report casesMaría Taboada, Verónica Alvarez, Diego Martínez, et al.Database : the Journal of Biological Databases and Curation|October 29, 2015
PhenoMiner: from text to a database of phenotypes associated with OMIM diseasesNigel Collier, Tudor Groza, Damian Smedley, et al.The International Journal of Biochemistry & Cell Biology|December 25, 2012
miR-181a promotes osteoblastic differentiation through repression of TGF-β signaling moleculesRaghu Bhushan, Johannes Grünhagen, Jessica Becker, et al.Molecular Vision|December 15, 2007
A recurrent FBN1 mutation in an autosomal dominant ectopia lentis family of Indian originVanita Vanita, Jai Rup Singh, Daljit Singh, et al.Health Informatics Journal|January 8, 2015
Mapping longitudinal studies to risk factors in an ontology for dementiaMark Roantree, Jim O' Donoghue, Noel O' Kelly, et al.Journal of Alzheimer'S Disease : JAD|August 20, 2019
Modifiable Risk Factors Explain Socioeconomic Inequalities in Dementia Risk: Evidence from a Population-Based Prospective Cohort StudyKay Deckers, Dorina Cadar, Martin P J van Boxtel, et al.Pageof 58