Cite
HARVARD Citation
Yamoto, K. et al. (2017). De novo IGF2 mutation on the paternal allele in a patient with Silver–Russell syndrome and ectrodactyly. Human mutation. 38 (8), pp. 953-958. [Online].
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Yamoto, K. et al. (2017). De novo IGF2 mutation on the paternal allele in a patient with Silver–Russell syndrome and ectrodactyly. Human mutation. 38 (8), pp. 953-958. [Online].