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Molecular Genetics & Genomic Medicine|January 12, 2019
RNA-Seq detects a SAMD12-EXT1 fusion transcript and leads to the discovery of an EXT1 deletion in a child with multiple osteochondromasGavin R Oliver, Patrick R Blackburn, Marissa S Ellingson, et al.
Mayo Clinic Proceedings|July 2, 2019
Clinical Applications and Utility of a Precision Medicine Approach for Patients With Unexplained CytopeniasAbhishek A Mangaonkar, Alejandro Ferrer, Filippo Pinto E Vairo, et al.
European Child & Adolescent Psychiatry|February 9, 2021
Heterogeneity of social cognitive and language functions in children at familial high-risk of severe mental illness; The Danish High Risk and Resilience Study VIA 7Camilla Jerlang Christiani, Nicoline Hemager, Ditte Ellersgaard, et al.
The Journal of Sexual Medicine|November 1, 2014
Acute nonarteritic anterior ischemic optic neuropathy and exposure to phosphodiesterase type 5 inhibitorsUlka B Campbell, Alexander M Walker, Michael Gaffney, et al.
Scientific Reports|June 12, 2023
T cell repertoire breadth is associated with the number of acute respiratory infections in the LoewenKIDS birth cohortLisa Paschold, Cornelia Gottschick, Susan Langer, et al.
Laboratory Hematology : Official Publication of the International Society for Laboratory Hematology|March 29, 2003
International Council for Standardization in Haematology (ICSH) recommendations for "surrogate reference" method for the packed cell volumeB S Bull, K Fujimoto, B Houwen, et al.
Brain Sciences|August 6, 2021
Expansion of the Genotypic and Phenotypic Spectrum of WASF1-Related Neurodevelopmental DisorderSiddharth Srivastava, Erica L Macke, Lindsay C Swanson, et al.
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