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American Journal of Medical Genetics. Part A|June 1, 2021
Recurrent KCNT2 missense variants affecting p.Arg190 result in a recognizable phenotypeAdam Jackson, Siddharth Banka, Helen Stewart, et al.
European Journal of Medical Genetics|December 31, 2017
The TBR1-related autistic-spectrum-disorder phenotype and its clinical spectrumJ H McDermott, D D D Study, J Clayton-Smith, et al.
Clinical Dysmorphology|March 14, 2007
Cerebro-facio-thoracic dysplasia: expanding the phenotypeDeirdre Cilliers, Yasemin Alanay, Koray Boduroglu, et al.
Public Health Genomics|October 9, 2015
Collaborative Crowdsourcing for the Diagnosis of Rare Genetic Syndromes: The DYSCERNE ExperienceSofia Douzgou, Yiannis A Pollalis, Athanassios Vozikis, et al.
Journal of Medical Imaging (Bellingham, Wash.)|October 2, 2019
Erratum: Prostate cancer detection from multi-institution multiparametric MRIs using deep convolutional neural networks system (Erratum)Yohan Sumathipala, Nathan Lay, Baris Turkbey, et al.
Journal of Medical Imaging (Bellingham, Wash.)|March 7, 2019
Prostate cancer detection from multi-institution multiparametric MRIs using deep convolutional neural networksYohan Sumathipala, Nathan Lay, Baris Turkbey, et al.
Journal of Molecular Biology|August 23, 2015
Septin 9 Exhibits Polymorphic Binding to F-Actin and Inhibits Myosin and Cofilin ActivityClayton Smith, Lee Dolat, Dimitrios Angelis, et al.
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