AAAAAA

   
Results: 1-5 |
Results: 5

Authors: ARDUINO C FERRONE M BRUSCO A GARNERONE S FONTANA D ROLLE L CARBONARA AO
Citation: C. Arduino et al., CONGENITAL BILATERAL ABSENCE OF VAS-DEFERENS WITH A NEW MISSENSE MUTATION (P499A) IN THE CFTR GENE, Clinical genetics, 53(3), 1998, pp. 202-204

Authors: RESTAGNO G ROMERO N RICHARD I BECKMANN JS PAGLIANO M FERRONE M CARBONARA A MERLINI L
Citation: G. Restagno et al., PRENATAL-DIAGNOSIS OF LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE 2A, Neuromuscular disorders, 6(3), 1996, pp. 173-176

Authors: RESTAGNO G FERRONE M DORIGUZZI C PALMUCCI L MONGINI T CARBONARA A
Citation: G. Restagno et al., CARRIER DETECTION OF DUCHENNE MUSCULAR-DYSTROPHY THROUGH ANALYSIS OF DNA FROM DECIDUOUS TEETH OF A DEAD AFFECTED CHILD, Prenatal diagnosis, 15(7), 1995, pp. 672-674

Authors: MILLER J KNORR R FERRONE M HOUDEI R CARRON CP DUSTIN ML
Citation: J. Miller et al., INTERCELLULAR-ADHESION MOLECULE-1 DIMERIZATION AND ITS CONSEQUENCES FOR ADHESION MEDIATED BY LYMPHOCYTE FUNCTION ASSOCIATED-1, The Journal of experimental medicine, 182(5), 1995, pp. 1231-1241

Authors: DORIGUZZI C PALMUCCI L MONGINI T CHIADOPIAT L RESTAGNO G FERRONE M
Citation: C. Doriguzzi et al., EXERCISE INTOLERANCE AND RECURRENT MYOGLOBINURIA AS THE ONLY EXPRESSION OF XP21 BECKER TYPE MUSCULAR-DYSTROPHY, Journal of neurology, 240(5), 1993, pp. 269-271
Risultati: 1-5 |