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The Journal of Clinical Investigation|November 1, 1974
Immunological studies of the human placenta. Characterization of immunoglobulins on trophoblastic basement membranesW P Faulk, M Jeannet, W D Creighton, et al.Clinical Genetics|December 1, 1992
Analysis of CA/GT microsatellite polymorphism in IVS8 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene: a study of Italian CF familiesG Restagno, S Garnerone, C Gennaro, et al.Human Genetics|January 1, 1981
Dicentric Y chromosome in a patient with gonadal dysgenesis and seminomaG Ponzio, M DeMarchi, A Carbonara, et al.Prenatal Diagnosis|July 1, 1995
Carrier detection of Duchenne muscular dystrophy through analysis of DNA from deciduous teeth of a dead affected childG Restagno, M Ferrone, C Doriguzzi, et al.European Journal of Ophthalmology|April 1, 1996
Analysis of the rhodopsin and peripherin/RDS gene in two families with pattern dystrophy of the retinal pigment epitheliumS Daniele, G Restagno, C Daniele, et al.Journal of Cancer Research and Clinical Oncology|January 1, 1980
G1 heavy chain disease: clinicopathological, ultrastructural and immunochemical study of a new caseA Stramignoni, A Carbonara, W Paolino, et al.International Journal of Clinical & Laboratory Research|January 1, 1994
Validation of IgA1 and IgA2 measurements by a solid-phase immunoradiometric assay in serum and secretionsS Depelchin, J P Dehennin, A Bottaro, et al.Journal of the Neurological Sciences|September 1, 1992
Dilating cardiomyopathy as the expression of Xp21 Becker type muscular dystrophyL Palmucci, C Doriguzzi, T Mongini, et al.Haematologica|July 1, 1992
Carrier detection for prenatal diagnosis of hemophilia A in Italian familiesN Cappello, G Restagno, S Garnerone, et al.Gut|August 1, 1983
HLA-DR3 and DR7 in coeliac disease: immunogenetic and clinical aspectsM Demarchi, A Carbonara, N Ansaldi, et al.Pageof 3