AAAAAA

   
Results: 1-6 |
Results: 6

Authors: Seidman, JG Seidman, C
Citation: Jg. Seidman et C. Seidman, The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms, CELL, 104(4), 2001, pp. 557-567

Authors: Clapham, D Michel, T Seidman, C
Citation: D. Clapham et al., In Memorium - Eva Neer, J MOL CEL C, 33(8), 2001, pp. 1393-1394

Authors: Seidman, C Patrick, K Scutchfield, FD
Citation: C. Seidman et al., A tribute to Abram S. Benenson, MD, AM J PREV M, 18(2), 2000, pp. 107-108

Authors: Eavey, RD Manolis, EN Lubianca, J Merchant, S Seidman, JG Seidman, C
Citation: Rd. Eavey et al., Mutations in COCH (formerly Coch5b2) cause DFNA9, ADV OTO-RH, 56, 2000, pp. 101-102

Authors: Seidman, C
Citation: C. Seidman, Hypertrophic cardiomyopathy: from man to mouse, J CLIN INV, 106(9), 2000, pp. S9-S13

Authors: Blanchard, E Seidman, C Seidman, JG LeWinter, M Maughan, D
Citation: E. Blanchard et al., Altered crossbridge kinetics in the alpha MHC403/+ mouse model of familialhypertrophic cardiomyopathy, CIRCUL RES, 84(4), 1999, pp. 475-483
Risultati: 1-6 |