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Molecular Genetics & Genomic Medicine|December 19, 2020
RB1CC1 duplication and aberrant overexpression in a patient with schizophrenia: further phenotype delineation and proposal of a pathogenetic mechanismEdoardo Errichiello, Roberto Giorda, Antonella Gambale, et al.
Translational Psychiatry|September 16, 2022
Maternal and infant NR3C1 and SLC6A4 epigenetic signatures of the COVID-19 pandemic lockdown: when timing mattersSarah Nazzari, Serena Grumi, Fabiana Mambretti, et al.
Journal of Neurochemistry|April 11, 2007
DNA methylation regulates tissue-specific expression of Shank3Silvana Beri, Noemi Tonna, Giorgia Menozzi, et al.
European Journal of Human Genetics : EJHG|September 25, 2008
A familial inverted duplication/deletion of 2p25.1-25.3 provides new clues on the genesis of inverted duplicationsMaria Clara Bonaglia, Roberto Giorda, Angelo Massagli, et al.
Molecular Cytogenetics|November 12, 2013
8q12 microduplication including CHD7: clinical report on a new patient with Duane retraction syndrome type 3Anna Baroncini, Sara Bertuzzo, Rita Quarantini, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines|August 19, 2009
The role played by the interaction between genetic factors and attachment in the stress response in infancyAlessandra Frigerio, Elisa Ceppi, Marianna Rusconi, et al.
Journal of Human Genetics|October 26, 2017
The role of READ1 and KIAA0319 genetic variations in developmental dyslexia: testing main and interactive effectsVittoria Trezzi, Diego Forni, Roberto Giorda, et al.
Early Human Development|December 12, 2018
Telomere length and salivary cortisol stress reactivity in very preterm infantsLivio Provenzi, Roberto Giorda, Monica Fumagalli, et al.
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