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Schizophrenia Research|January 16, 2019
The impact of gender and childhood abuse on age of psychosis onset, psychopathology and needs for care in psychosis patientsCarla Comacchio, Louise M Howard, Chiara Bonetto, et al.
Human Molecular Genetics|February 5, 2008
Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumourFlavia Cerrato, Angela Sparago, Gaetano Verde, et al.
Scientific Reports|June 30, 2018
Publisher Correction: TGF-β concentrations and activity are down-regulated in the aqueous humor of patients with neovascular age-related macular degenerationGian Marco Tosi, Giovanni Neri, Elena Caldi, et al.
ACS Applied Materials & Interfaces|December 17, 2024
Molybdenum Disulfide/Diselenide-Laser-Induced Graphene-Glycine Oxidase Composite for Electrochemical Sensing of GlyphosateRayhane Zribi, Zachary T Johnson, Griffin Ellis, et al.
American Journal of Medical Genetics. Part A|November 18, 2008
A previously undescribed syndrome combining fibular agenesis/hypoplasia, oligodactylous clubfeet, anonychia/ungual hypoplasia, and other defectsSilvana C Santos, Eliete Pardono, Maria Ione Ferreira da Costa, et al.
American Journal of Medical Genetics. Part A|May 13, 2006
Split-hand/split-foot malformation 3 (SHFM3) at 10q24, development of rapid diagnostic methods and gene expression from the regionRobert Lyle, Uppala Radhakrishna, Jean-Louis Blouin, et al.
Scientific Reports|May 26, 2018
TGF-β concentrations and activity are down-regulated in the aqueous humor of patients with neovascular age-related macular degenerationGian Marco Tosi, Giovanni Neri, Elena Caldi, et al.
NAR Molecular Medicine|February 4, 2026
FMR1 RNA interaction with DNMT1 blocks DNA methylation at the FMR1 locusVeronica Nobile, Benedetta Niccolini, Cecilia Pucci, et al.
Pediatrics|September 3, 2014
Cardio-facio-cutaneous syndrome: clinical features, diagnosis, and management guidelinesMary Ella M Pierpont, Pilar L Magoulas, Saleh Adi, et al.
Human Mutation|May 4, 2011
Characterization of a novel transcript of the EHMT1 gene reveals important diagnostic implications for Kleefstra syndromeWilly M Nillesen, Helger G Yntema, Marco Moscarda, et al.
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