PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy.
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V. Frey | J. Harpey | C. Cruaud | B. Estournet | K. Tryggvason | M. Mora | A. Helbling-Leclerc | B. Hainque | H. Topaloglu | Yi He | M. Fardeau | P. Guicheney | K. Schwartz | F. Tomé | P. Richard | L. Merlini | N. Vignier | X. Zhang | C. Haenggeli | Xu Zhang | Y. He | A. Barois | H. Topaloğlu