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HARVARD Citation
Fontana, P. et al. (2017). SNORD116 deletions cause Prader‐Willi syndrome with a mild phenotype and macrocephaly. Clinical genetics. 92 (4), pp. 440-443. [Online].
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Fontana, P. et al. (2017). SNORD116 deletions cause Prader‐Willi syndrome with a mild phenotype and macrocephaly. Clinical genetics. 92 (4), pp. 440-443. [Online].