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PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy
- Guicheney, P (author)
- Vignier, N (author)
- Zhang, X (author)
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- He, Y (author)
- Cruaud, C (author)
- Frey, V (author)
- Helbling-Leclerc, A (author)
- Richard, P (author)
- Estournet, B (author)
- Merlini, L (author)
- Topaloglu, H (author)
- Mora, M (author)
- Harpey, JP (author)
- Haenggeli, CA (author)
- Barois, A (author)
- Hainque, B (author)
- Schwartz, K (author)
- Tome, FMS (author)
- Fardeau, M (author)
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- (creator_code:org_t)
- BMJ, 1998
- 1998
- English.
- In: Journal of medical genetics. - : BMJ. - 0022-2593 .- 1468-6244. ; 35:3, s. 211-217
- Journal article (peer-reviewed)
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- art (subject category)
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- Guicheney, P
- Vignier, N
- Zhang, X
- He, Y
- Cruaud, C
- Frey, V
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- Helbling-Leclerc ...
- Richard, P
- Estournet, B
- Merlini, L
- Topaloglu, H
- Mora, M
- Harpey, JP
- Haenggeli, CA
- Barois, A
- Hainque, B
- Schwartz, K
- Tome, FMS
- Fardeau, M
- Tryggvason, K
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- Journal of medic ...
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- Karolinska Institutet
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