A prenatal diagnosis and genetics study of five pedigrees in the Chinese population with Xp22.31 microduplication
Copy number variations (CNVs) can contribute to human phenotype, phenotypic diversity and disease susceptibility, while others may benign. In the current study, an attempt to investigate the pathogenicity of C...
Source: Molecular Cytogenetics - Category: Molecular Biology Authors: Jianlong Zhuang, Yuanbai Wang, Shuhong Zeng, Chunling Lv, Yiming Lin and Yuying Jiang Tags: Research Source Type: research