AAAAAA

   
Results: 1-5 |
Results: 5

Authors: LI H CHEN QY MOSS AJ ROBINSON J GOYTIA V PERRY JC VINCENT GM PRIORI SG LEHMANN MH DENFIELD SW DUFF D KAINE S SHIMIZU W SCHWARTZ PJ WANG Q TOWBIN JA
Citation: H. Li et al., NEW MUTATIONS IN THE KVLQT1 POTASSIUM CHANNEL THAT CAUSE LONG-QT SYNDROME, Circulation, 97(13), 1998, pp. 1264-1269

Authors: ORTIZLOPEZ R LI H SU J GOYTIA V TOWBIN JA
Citation: R. Ortizlopez et al., EVIDENCE FOR A DYSTROPHIN MISSENSE MUTATION AS A CAUSE OF X-LINKED DILATED CARDIOMYOPATHY, Circulation, 95(10), 1997, pp. 2434-2440

Authors: SCHULTZ KR GAJARSKI R PORTER P GOYTIA V BACHINSKI L ROBERTS R PIGNATELLI R TOWBIN JA
Citation: Kr. Schultz et al., MAPPING OF A FAMILIAL DILATED CARDIOMYOPATHY GENE AND EVIDENCE FOR GENETIC-HETEROGENEITY, Pediatric research, 39(4), 1996, pp. 204-204

Authors: BOWLES KR GAJARSKI R PORTER P GOYTIA V BACHINSKI L ROBERTS R PIGNATELLI R TOWBIN JA
Citation: Kr. Bowles et al., GENE-MAPPING OF FAMILIAL AUTOSOMAL-DOMINANT DILATED CARDIOMYOPATHY TOCHROMOSOME 1OQ21-23, The Journal of clinical investigation, 98(6), 1996, pp. 1355-1360

Authors: SCHULTZ KR GAJARSKI RJ PIGNATELLI R GOYTIA V ROBERTS R BACHINSKI L TOWBIN JA
Citation: Kr. Schultz et al., GENETIC-HETEROGENEITY IN FAMILIAL DILATED CARDIOMYOPATHY, Biochemical and molecular medicine, 56(2), 1995, pp. 87-93
Risultati: 1-5 |