Effects of dexamethasone on the growth of cultured rabbit articular chondrocytes:relation with the nuclear glucocorticoid-receptor complex.

od Hainque, B, Dominice, J, Jaffray, P, Ronot, X, Adolphe, M
Izdano 1987

First description of germline mosaicism in familial hypertrophic cardiomyopathy

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

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

od Charron, P, Heron, D, Gargiulo, M, Richard, P, Dubourg, O, Desnos, M, Bouhour, J, Feingold, J, Carrier, L, Hainque, B, Schwartz, K, Komajda, M
Izdano 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

od 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.
Izdano 1999

Possible founder effect of rapsyn N88K mutation and identification of novel rapsyn mutations in congenital myasthenic syndromes

od Richard, P, Gaudon, K, Andreux, F, Yasaki, E, Prioleau, C, Bauche, S, Barois, A, Ioos, C, Mayer, M, Routon, M, Mokhtari, M, Leroy, J, Fournier, E, Hainque, B, Koenig, J, Fardeau, M, Eymard, B, Hantai, D
Izdano 2003

PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy.

od Guicheney, P, Vignier, N, Zhang, X, He, Y, Cruaud, C, Frey, V, Helbling-Leclerc, A, Richard, P, Estournet, B, Merlini, L, Topaloglu, H, Mora, M, Harpey, J P, Haenggeli, C A, Barois, A, Hainque, B, Schwartz, K, Tomé, F M, Fardeau, M, Tryggvason, K
Izdano 1998