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Clinical Dysmorphology|July 29, 2016
Rubinstein-Taybi syndrome type 2: report of nine new cases that extend the phenotypic and genotypic spectrumMark J Hamilton, Ruth Newbury-Ecob, Muriel Holder-Espinasse, et al.
Journal of Chemical Education|February 14, 2020
Industry-Informed Workshops to Develop Graduate Skill Sets in the Circular Economy Using Systems ThinkingLouise Summerton, James H Clark, Glenn A Hurst, et al.
Neurology. Genetics|May 31, 2021
Diagnosing Mitochondrial Disorders Remains Challenging in the Omics EraPatrick Forny, Emma Footitt, James E Davison, et al.
Nature Communications|January 14, 2017
TNFα drives pulmonary arterial hypertension by suppressing the BMP type-II receptor and altering NOTCH signallingLiam A Hurst, Benjamin J Dunmore, Lu Long, et al.
American Journal of Medical Genetics. Part A|July 14, 2006
Clinical dividends from the molecular genetic diagnosis of craniosynostosisAndrew O M Wilkie, Elena G Bochukova, Ruth M S Hansen, et al.
Frontiers in Endocrinology|June 2, 2012
Early Diagnosis of Werner's Syndrome Using Exome-Wide Sequencing in a Single, Atypical PatientEleanor Raffan, Liam A Hurst, Saeed Al Turki, et al.
Cancer Prevention Research (Philadelphia, Pa.)|June 3, 2015
Activation of the PI3K/Akt/mTOR and MAPK Signaling Pathways in Response to Acute Solar-Simulated Light Exposure of Human SkinYira Bermudez, Steven P Stratton, Clara Curiel-Lewandrowski, et al.
American Journal of Medical Genetics. Part A|July 11, 2007
Clinical dividends from the molecular genetic diagnosis of craniosynostosisAndrew O M Wilkie, Elena G Bochukova, Ruth M S Hansen, et al.
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