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Developmental Medicine and Child Neurology|January 1, 1993
Diagnosis of DMD carrier status in a family with no known affected malesF Muntoni, A Mateddu, M Cau, et al.European Journal of Dental Education : Official Journal of the Association for Dental Education in Europe|October 13, 2017
Perception of Special Needs Dentistry education and practice amongst Australian dental auxiliary studentsG L Borromeo, M S Ahmad, S Buckley, et al.British Journal of Haematology|June 1, 1995
A promoter mutation, C-->T at position -92, leading to silent beta-thalassaemiaM C Rosatelli, V Faà, A Meloni, et al.Nouvelle Revue Francaise D'Hematologie|January 1, 1986
Genetic control of the proportion of gamma chains of human fetal haemoglobinM Arbane, L Morle, E Dessi, et al.Archives of Disease in Childhood|January 1, 1985
Perinatal hepatitis B virus detection by hepatitis B virus-DNA analysisS De Virgiliis, F Frau, G Sanna, et al.European Journal of Pediatrics|April 1, 1988
Human immunodeficiency virus infection in multi-transfused patients with thalassaemia majorP E Manconi, C Dessí, G Sanna, et al.Journal of Magnetic Resonance Imaging : JMRI|October 7, 2018
Anatomical location, sex, and age influence murine arterial circumferential cyclic strain before and during dobutamine infusionPaige E Castle, Ulrich M Scheven, A Colleen Crouch, et al.Genetic Testing|February 24, 2001
Delineation of the spectrum of Wilson disease mutations in the Greek population and the identification of six novel mutationsG Loudianos, M Lovicu, P Solinas, et al.British Journal of Haematology|June 1, 1992
A beta-thalassaemia phenotype not linked to the beta-globin cluster in an Italian familyS Murru, G Loudianos, S Porcu, et al.The Journal of Pediatrics|August 1, 1995
A specific cystic fibrosis mutation (T3381) associated with the phenotype of isolated hypotonic dehydrationG B Leoni, S Pitzalis, R Podda, et al.Pageof 37