Cite
HARVARD Citation
Prontera, P. et al. (n.d.). A New Homozygous IGF1R Variant Defines a Clinically Recognizable Incomplete Dominant form of SHORT Syndrome. Human mutation. 36 (11), pp. 1043-1047. [Online].
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Prontera, P. et al. (n.d.). A New Homozygous IGF1R Variant Defines a Clinically Recognizable Incomplete Dominant form of SHORT Syndrome. Human mutation. 36 (11), pp. 1043-1047. [Online].