Associated Papers
Analysis of clinical and genetic characteristics in 10 Chinese individuals with Cornelia de Lange syndrome and literature review.
Liu C et al.
Molecular Genetics & Genomic Medicine, 2020
[Identification and prenatal diagnosis of a novel NIPBL mutation underlying Cornelia De Lange syndrome].
Bai Z et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2019
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