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Human Heredity|September 28, 2006
SNP-based analysis of genetic substructure in the German populationMichael Steffens, Claudia Lamina, Thomas Illig, et al.American Journal of Human Genetics|February 7, 2012
Haploinsufficiency of a spliceosomal GTPase encoded by EFTUD2 causes mandibulofacial dysostosis with microcephalyMatthew A Lines, Lijia Huang, Jeremy Schwartzentruber, et al.Nature Communications|December 14, 2017
Identification and characterization of two functional variants in the human longevity gene FOXO3Friederike Flachsbart, Janina Dose, Liljana Gentschew, et al.Nature Communications|January 18, 2018
Publisher Correction: Identification and characterization of two functional variants in the human longevity gene FOXO3Friederike Flachsbart, Janina Dose, Liljana Gentschew, et al.Human Genetics|June 23, 2021
Genome sequencing in families with congenital limb malformationsJonas Elsner, Martin A Mensah, Manuel Holtgrewe, et al.Journal of Infection and Public Health|March 8, 2024
Prevalence of infectious diseases, immunity to vaccine-preventable diseases and chronic medical conditions among Ukrainian refugees in Germany - A cross sectional study from the German Network University Medicine (NUM)Folke Brinkmann, Anette Friedrichs, Georg Mn Behrens, et al.Infection|July 31, 2025
Performance of whole blood interferon-γ release assays in SARS-CoV-2 and tuberculosis is age dependentTobias Rothoeft, Anna Teresa Hoffmann, Christoph Maier, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 25, 2018
TANGO2: expanding the clinical phenotype and spectrum of pathogenic variantsJennifer N Dines, Katie Golden-Grant, Amy LaCroix, et al.European Journal of Human Genetics : EJHG|January 22, 2009
An evaluation of the genetic-matched pair study design using genome-wide SNP data from the European populationTimothy Tehua Lu, Oscar Lao, Michael Nothnagel, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 18, 2018
Correction: TANGO2: expanding the clinical phenotype and spectrum of pathogenic variantsJennifer N Dines, Katie Golden-Grant, Amy LaCroix, et al.Pageof 28