Laura J Russell
Associate Professor, Department of Human Genetics
![Laura J Russell Laura J Russell](/sbms/files/sbms/styles/medium_focal__220_x_220_/public/laura_russell.jpg?itok=sTgtZ9f_)
Clinical delineation of birth defects and of inherited disorders associated with intellectual disability; genodermatoses;
Der Kaloustian, VM, Russell, L, Aradhya, S, Richard, G, Rosenblatt, B, Melançon, S. A de novo 2.1-Mb deletion of 13q12.11 in a child with developmental delay and minor dysmorphic features. Am. J. Med. Genet. 55(10): 2538-2542, 2011.
Lévesque, S, Lambert, M, Karalis, A, Melançon, S, Russell, L, Braverman, N. Short-Term Outcome of Propionic Aciduria Treated at Presentation with N-Carbamylglutamate: A Retrospective Review of Four Patients. J Inherit Metab Dis, in press.
Vanneste R, Chiu S-M, Russell L, Fitzpatrick J. Effects of Second Language Usage on Genetic Counseling Training and Supervision. J Genet Counsel 2012; DOI 10.1007/s10897-012-9509-7.