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European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|August 1, 2008
Correlation between GJB2 mutations and audiological deficits: personal experiencePasqualina M Picciotti, Roberta Pietrobono, Giovanni Neri, et al.
Journal of Environmental Sciences (China)|November 3, 2023
A novel 2D-GO@WS2 electrochemical platform for the determination of thiram fungicideKhouloud Abid, Daniela Iannazzo, Consuelo Celesti, et al.
Epigenetics & Chromatin|March 26, 2016
Genome-wide methylation analysis demonstrates that 5-aza-2-deoxycytidine treatment does not cause random DNA demethylation in fragile X syndrome cellsElisabetta Tabolacci, Giorgia Mancano, Stella Lanni, et al.
Autism Research : Official Journal of the International Society for Autism Research|August 15, 2009
Further evidence that the rs1858830 C variant in the promoter region of the MET gene is associated with autistic disorderPamela B Jackson, Luigi Boccuto, Cindy Skinner, et al.
ACS Omega|April 27, 2026
Graphene Dot-ZnO Hybrid Nanostructures as High-Performance Chemiresistive Sensors for H2S DetectionFederica Bucolo, Daniela Iannazzo, Nesrine Hafiene, et al.
Marine Environmental Research|June 5, 2004
Evaluation of ecotoxicological effects of endocrine disrupters during a four-year survey of the Mediterranean population of swordfish (Xiphias gladius)M Cristina Fossi, Silvia Casini, Letizia Marsili, et al.
Angewandte Chemie (International Ed. in English)|October 2, 2012
Room-temperature hydrogen sensing with heteronanostructures based on reduced graphene oxide and tin oxidePatrícia A Russo, Nicola Donato, Salvatore Gianluca Leonardi, et al.
American Journal of Medical Genetics|July 13, 2002
HOXD13 polyalanine tract expansion in classical synpolydactyly type VordingborgKlaus Wilbrandt Kjaer, Jess Hedeboe, Merete Bugge, et al.
American Journal of Medical Genetics|September 20, 2002
FG syndrome: linkage analysis in two families supporting a new gene localization at Xp22.3 [FGS3]Sabine Dessay, Marie Pierre Moizard, Jean Louis Gilardi, et al.
Fetal and Pediatric Pathology|November 9, 2011
Unilateral sclerocornea and tracheal stenosis: unusual findings in a patient with Goldenhar anomalyLarissa V Furtado, Angelica R Putnam, David H Viskochil, et al.
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