Cite
HARVARD Citation
Slavotinek, A. et al. (2005). Fryns syndrome phenotype caused by chromosome microdeletions at 15q26.2 and 8p23.1. Journal of medical genetics. 42 (9), pp. 730-736. [Online].
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Slavotinek, A. et al. (2005). Fryns syndrome phenotype caused by chromosome microdeletions at 15q26.2 and 8p23.1. Journal of medical genetics. 42 (9), pp. 730-736. [Online].