Cite
HARVARD Citation
Izumi, K. et al. (n.d.). Endocrine phenotype of 6q16.1–q21 deletion involving SIM1 and Prader–Willi syndrome‐like features. American journal of medical genetics. 161 (12), pp. 3137-3143. [Online].
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Izumi, K. et al. (n.d.). Endocrine phenotype of 6q16.1–q21 deletion involving SIM1 and Prader–Willi syndrome‐like features. American journal of medical genetics. 161 (12), pp. 3137-3143. [Online].