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Yi Esther SU
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汉语自闭症学前儿童语言表达能力实证研究
Journal:语言战略研究 (CSSCI扩展）
Translation or Not:no
Pre One:
A novel proximal 3q29 chromosome microdeletion in a Chinese patient with Chiari malformation type II and Sprengel's deformity
Next One:
Whole-exome sequencing identifies a Novel SCN5A mutation (C335R) in a Chinese family with arrhythmia
