Showing results (141-150 of 325) with videos related to

Sort By:
Pageof 33
Medicine|December 20, 2015
Corneal Complications During and After Vitrectomy for Retinal Detachment in Photorefractive Keratectomy Treated EyesGian Marco Tosi, Stefano Baiocchi, Angelo Balestrazzi, et al.
International Journal of Biological Macromolecules|November 4, 2023
New fluorescent Schiff base modified nanocellulose-based chemosensors for the selective detection of Fe3+, Zn2+ and Cu2+ in semi-aqueous media and application in seawater sampleSarah Ben Haj Fraj, Angelo Ferlazzo, Jamal El Haskouri, et al.
American Journal of Medical Genetics. Part A|January 28, 2003
Cryptic t(1;12)(q44;p13.3) translocation in a previously described syndrome with polymicrogyria, segregating as an apparently X-linked traitMarcella Zollino, Cesare Colosimo, Orsetta Zuffardi, et al.
Pharmacogenetics and Genomics|July 16, 2008
Modest reactivation of the mutant FMR1 gene by valproic acid is accompanied by histone modifications but not DNA demethylationElisabetta Tabolacci, Ivana De Pascalis, Maria Accadia, et al.
Retina (Philadelphia, Pa.)|January 14, 2017
VITREOUS INCARCERATION IN SCLEROTOMIES AFTER VALVED 23-, 25-, OR 27-GAUGE AND NONVALVED 23- OR 25-GAUGE MACULAR SURGERYGian Marco Tosi, Alex Malandrini, Gabriele Cevenini, et al.
Materials (Basel, Switzerland)|July 13, 2024
Conductometric H2S Sensors Based on TiO2 NanoparticlesYassine Alaya, Malek Madani, Noureddine Bouguila, et al.
Biosensors|April 8, 2020
Electrochemical Sensing of Serotonin by a Modified MnO2-Graphene ElectrodeLavanya Nehru, Sekar Chinnathambi, Enza Fazio, et al.
American Journal of Medical Genetics. Part A|May 20, 2011
A deletion 13q34/duplication 14q32.2-14q32.33 syndrome diagnosed 50 years after neonatal presentation as infantile hypercalcemiaPhilip D Pallister, Adam B Pallister, Sarah South, et al.
American Journal of Medical Genetics. Part A|May 8, 2013
Elements of morphology: standard terminology for the external genitaliaRaoul C M Hennekam, Judith E Allanson, Leslie G Biesecker, et al.
European Journal of Human Genetics : EJHG|May 3, 2012
TRAPPC9-related autosomal recessive intellectual disability: report of a new mutation and clinical phenotypeGiuseppe Marangi, Vincenzo Leuzzi, Filippo Manti, et al.
Pageof 33