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HARVARD Citation
Myring, J. et al. (1992). Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophy.. Journal of medical genetics. 29 (11), pp. 785-788. [Online].
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Myring, J. et al. (1992). Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophy.. Journal of medical genetics. 29 (11), pp. 785-788. [Online].