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European Journal of Medical Genetics|January 30, 2008
Concurrent transposition of distal 6p and 20q to the 22q telomere: a recurrent benign chromosomal variantMaria Clara Bonaglia, Roberto Giorda, Silvana Beri, et al.Developmental Psychobiology|December 29, 2021
The role of maternal touch in the association between SLC6A4 methylation and stress response in very preterm infantsIsabella Lucia Chiara Mariani Wigley, Eleonora Mascheroni, Camilla Fontana, et al.Frontiers in Behavioral Neuroscience|May 6, 2015
Pain-related stress during the Neonatal Intensive Care Unit stay and SLC6A4 methylation in very preterm infantsLivio Provenzi, Monica Fumagalli, Ida Sirgiovanni, et al.Acta Paediatrica (Oslo, Norway : 1992)|November 1, 2019
Pain-related increase in serotonin transporter gene methylation associates with emotional regulation in 4.5-year-old preterm-born childrenLivio Provenzi, Monica Fumagalli, Giunia Scotto di Minico, et al.European Journal of Human Genetics : EJHG|March 21, 2009
Complex pathogenesis of Hirschsprung's disease in a patient with hydrocephalus, vesico-ureteral reflux and a balanced translocation t(3;17)(p12;q11)Paola Griseri, Yvonne Vos, Roberto Giorda, et al.Human Genetics|September 1, 2005
Direct duplication 12p11.21-p13.31 mediated by segmental duplications: a new recurrent rearrangement?Manuela De Gregori, Tiziano Pramparo, Luigi Memo, et al.European Child & Adolescent Psychiatry|October 16, 2014
GRIN2B predicts attention problems among disadvantaged childrenValentina Riva, Marco Battaglia, Maria Nobile, et al.Molecular Cancer|August 1, 2009
The tumor suppressor gene TRC8/RNF139 is disrupted by a constitutional balanced translocation t(8;22)(q24.13;q11.21) in a young girl with dysgerminomaStefania Gimelli, Silvana Beri, Harry A Drabkin, et al.Human Genetics|June 2, 2009
Different molecular mechanisms causing 9p21 deletions in acute lymphoblastic leukemia of childhoodFrancesca Novara, Silvana Beri, Maria Ester Bernardo, et al.Brain Sciences|December 19, 2020
The Mediation Role of Dynamic Multisensory Processing Using Molecular Genetic Data in DyslexiaSara Mascheretti, Valentina Riva, Bei Feng, et al.Pageof 13