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[We report a Chinese girl diagnosed with Laron syndrome at age 1.9 years with height -4.9 SDS, basal GH 344 mIU/ml, IGF-I < 12 ng/ml, IGFBP-3 < 0.2 mg/ml, and undetectable GHBP/novel mutation of the GHR was identified at the donor splice site of intron 6.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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Gene-disease associations inferred from text-mining the literature.
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