DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Yamamoto T, Shimojima K, Yamazaki S, Ikeno K, Tohyama J.
A 16q12.2q21 deletion identified in a patient with developmental delay, epilepsy, short stature, and distinctive features.
Congenit Anom (Kyoto) 2016;
56 (06) 253-255
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