DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Nagahara K, Harada Y, Futami T, Takagi M, Nishimura G, Hasegawa Y.
A Japanese familial case of hypochondroplasia with a novel mutation in FGFR3.
Clin Pediatr Endocrinol 2016;
25 (03) 103-106
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