Experience from clinical genetics in hypertrophic cardiomyopathy: proposal for new diagnostic criteria in adult members of affected families.

Por McKenna, W. J., Spirito, P., Desnos, M., Dubourg, O., Komajda, M.
Publicado em 1997

Diagnostic value of markers of muscle degeneration in sporadic inclusion body myositis

Por Dubourg, O., Wanschitz, J., Maisonobe, T., Béhin, A., Allenbach, Y., Herson, S., Benveniste, O
Publicado em 2011

Linkage analysis of five fibrillar collagen loci in a large French Marfan syndrome family.

Por Boileau, C, Jondeau, G, Bonaiti, C, Coulon, M, Delorme, G, Dubourg, O, Bourdarias, J P, Junien, C
Publicado em 1990

The gene for spinal cerebellar ataxia 3 (SCA3) is located in a region of approximately 3 cM on chromosome 14q24.3-q32.2.

Por Stevanin, G, Cancel, G, Dürr, A, Chneiweiss, H, Dubourg, O, Weissenbach, J, Cann, H M, Agid, Y, Brice, A
Publicado em 1995

Familial hypertrophic cardiomyopathy. Microsatellite haplotyping and identification of a hot spot for mutations in the beta-myosin heavy chain gene.

Por Dausse, E, Komajda, M, Fetler, L, Dubourg, O, Dufour, C, Carrier, L, Wisnewsky, C, Bercovici, J, Hengstenberg, C, al-Mahdawi, S
Publicado em 1993

First description of germline mosaicism in familial hypertrophic cardiomyopathy

Por Forissier, J., Richard, P., Briault, S., Ledeuil, C., Dubourg, O., Charbonnier, B., Carrier, L., Moraine, C., Bonne, G., Komajda, M., Schwartz, K., Hainque, B.
Publicado em 2000

Relation between QT duration and maximal wall thickness in familial hypertrophic cardiomyopathy

Por Jouven, X, Hagege, A, Charron, P, Carrier, L, Dubourg, O, Langlard, J M, Aliaga, S, Bouhour, J B, Schwartz, K, Desnos, M, Komajda, M
Publicado em 2002

Genetic testing and genetic counselling in hypertrophic cardiomyopathy: the French experience

Por Charron, P, Heron, D, Gargiulo, M, Richard, P, Dubourg, O, Desnos, M, Bouhour, J, Feingold, J, Carrier, L, Hainque, B, Schwartz, K, Komajda, M
Publicado em 2002

Double heterozygosity for mutations in the β-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathy

Por Richard, P., Isnard, R., Carrier, L., Dubourg, O., Donatien, Y., Mathieu, B., Bonne, G., Gary, F., Charron, P., Hagege, A., Komajda, M., Schwartz, K., Hainque, B.
Publicado em 1999