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Orphanet Journal of Rare Diseases|March 15, 2025
Clinical and genetic aspects of Bardet-Biedl syndrome in adults in NorwayCecilie Fremstad Rustad, Ragnheidur Bragadottir, Kristian Tveten, et al.
European Journal of Human Genetics : EJHG|July 7, 2019
De novo substitutions of TRPM3 cause intellectual disability and epilepsyDavid A Dyment, Paulien A Terhal, Cecilie F Rustad, et al.
Molecular Genetics & Genomic Medicine|June 11, 2024
A monoallelic UXS1 variant associated with short-limbed short statureCecilie F Rustad, Paul Hoff Backe, Chunsheng Jin, et al.
European Journal of Human Genetics : EJHG|December 8, 2020
Benefits of clinical criteria and high-throughput sequencing for diagnosing children with syndromic craniosynostosisElin Tønne, Bernt Johan Due-Tønnessen, Inger-Lise Mero, et al.
Plos One|August 10, 2022
SARS-CoV-2 antibody persistence after five and twelve months: A cohort study from South-Eastern NorwayMarjut Sarjomaa, Lien My Diep, Chi Zhang, et al.
American Journal of Epidemiology|July 2, 2003
Mortality from cancer and other causes among airline cabin attendants in Europe: a collaborative cohort study in eight countriesHajo Zeeb, Maria Blettner, Ingo Langner, et al.
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