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Human Mutation|January 8, 2000
A new glucose 6 phosphate dehydrogenase variant G6PD Sinnai (34 G-->T). Mutations in brief no. 156. OnlineR Galanello, D Loi, C Sollaino, et al.
Human Mutation|January 8, 2000
Two novel mutations (10410 T-->G; 10296 del C) at carboxy-terminus of the dystrophin gene associated with mental retardation. Mutations in brief no. 149. OnlineM Cau, A Cao, D Loi, et al.
British Journal of Haematology|May 1, 1993
Normal individuals with high Hb A2 levelsD Gasperini, A Cao, L Paderi, et al.
IEEE Transactions on Biomedical Circuits and Systems|July 16, 2013
Peripheral neural activity recording and stimulation systemD Loi, C Carboni, G Angius, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 22, 2000
Elevation of serum creatine kinase as the only manifestation of an intragenic deletion of the dystrophin gene in three unrelated familiesM A Melis, M Cau, F Muntoni, et al.
Community Genetics|April 1, 2008
Thalassaemia and glucose-6-phosphate dehydrogenase screening in 13- to 14-year-old students of the Sardinian population: preliminary findingsA Cao, R Congiu, M C Sollaino, et al.
American Journal of Hematology|June 1, 1994
Genotype of subjects with borderline hemoglobin A2 levels: implication for beta-thalassemia carrier screeningR Galanello, S Barella, A Ideo, et al.
Medicinal Chemistry (Shariqah (United Arab Emirates))|July 3, 2015
Novel 3-substituted-2-oxoindoline-based N-hydroxypropenamides as histone deacetylase inhibitors and antitumor agentsDo T M Dung, Phan T P Dung, Dao T K Oanh, et al.
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