新生儿迪乔治综合征——诊断挑战

V. Carvalho
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引用次数: 0

摘要

DiGeorge综合征主要由22号染色体(22q11.2)微缺失引起,具有广泛的表型谱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
DiGeorge Syndrome In A Newborn - A Diagnostic Challenge
DiGeorge syndrome is mainly caused by microdeletion of chromosome 22 (22q11.2) and is characterized by a broad phenotypic spectrum.
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