Expanding the clinical spectrum of 19p13.3 microduplication syndrome
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https://www.ncbi.nlm.nih.gov/bioproject/PRJNA1161011
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资源简介：
The common clinical findings in patients with 19p13.3 duplication include intrauterine growth restriction, intellectual disability, language retardation, microcephaly, and special facial features. Herein, we report the case of a patient with 19p13.3 microduplication having novel clinical findings, specifically nephrotic syndrome.
创建时间：
2024-09-14
