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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.
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.
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.
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.
European Journal of Human Genetics : EJHG|February 11, 2005
A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexiaCecilia Marino, Roberto Giorda, Maria Luisa Lorusso, et al.
Human Genetics|July 13, 2010
Breakpoint determination of 15 large deletions in Peutz-Jeghers subjectsNicoletta Resta, Roberto Giorda, Rosanna Bagnulo, et al.
Journal of Affective Disorders|November 20, 2015
Effect of family structure and TPH2 G-703T on the stability of dysregulation profile throughout adolescenceMaria Nobile, Valentina Bianchi, Dario Monzani, et al.
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