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Author/Creator Hainque, B

2. Genetic testing and genetic counselling in hypertrophic cardiomyopathy: the French experience. Issue 10 (1st October 2002)

Authors:
Charron, P; Héron, D; Gargiulo, M; Richard, P; Dubourg, O; Desnos, M; Bouhour, J-B; Feingold, J; Carrier, L; Hainque, B; Schwartz, K; Komajda, M
Other Names:
group-author.
Journal:
Journal of medical genetics
Issue:
Volume 39:Issue 10(2002)
Page Start:
741
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy. Issue 3 (March 1998)

Authors:
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
Journal:
Journal of medical genetics
Issue:
Volume 35:Issue 3(1998)
Page Start:
211
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. Plakophilin 2A is the dominant isoform in human heart tissue: consequences for the genetic screening of arrhythmogenic right ventricular cardiomyopathy. Issue 10 (3rd March 2011)

Authors:
Gandjbakhch, E; Charron, P; Fressart, V; Lorin de la Grandmaison, G; Simon, F; Gary, F; Vite, A; Hainque, B; Hidden-Lucet, F; Komajda, M; Villard, E
Journal:
Heart
Issue:
Volume 97:Issue 10(2011)
Page Start:
844
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

5. Possible founder effect of rapsyn N88K mutation and identification of novel rapsyn mutations in congenital myasthenic syndromes. Issue 6 (1st June 2003)

Authors:
Richard, P; Gaudon, K; Andreux, F; Yasaki, E; Prioleau, C; Bauché, S; Barois, A; Ioos, C; Mayer, M; Routon, M C; Mokhtari, M; Leroy, J P; Fournier, E; Hainque, B; Koenig, J; Fardeau, M; Eymard, B; Hantaï, D
Journal:
Journal of medical genetics
Issue:
Volume 40:Issue 6(2003)
Page Start:
e81
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗