Molecular Cytogenetics | Home page

Molecular Cytogenetics | Home page



Molecular Cytogenetics

Official journal of

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1. A case of prenatal diagnosis of 18p deletion syndrome following noninvasive prenatal testing

   Authors:Ganye Zhao, Peng Dai, Shanshan Gao, Xuechao Zhao, Conghui Wang, Lina Liu and Xiangdong Kong

   Content type:Case Report

   21 December 2019

2. The variome concept: focus on CNVariome

   Authors:Ivan Y. Iourov, Svetlana G. Vorsanova and Yuri B. Yurov

   Content type:Hypothesis

   19 December 2019

3. A novel 14q13.1–21.1 deletion identified by CNV-Seq in a patient with brain-lung-thyroid syndrome, tooth agenesis and immunodeficiency

   Authors:Xuyun Hu, Jun Liu, Ruolan Guo, Jun Guo, Zhipeng Zhao, Wei Li, Baoping Xu and Chanjuan Hao

   Content type:Case Report

   19 December 2019

4. A prenatal diagnosis and genetics study of five pedigrees in the Chinese population with Xp22.31 microduplication

   Authors:Jianlong Zhuang, Yuanbai Wang, Shuhong Zeng, Chunling Lv, Yiming Lin and Yuying Jiang

   Content type:Research

   11 December 2019

5. Prenatal diagnosis of cri-du-chat syndrome by SNP array: report of twelve cases and review of the literature

   Authors:Jiasun Su, Huayu Fu, Bobo Xie, Weiliang Lu, Wei Li, Yuan Wei, Qiang Zhang, Shengkai Wei, Qiuli Chen, Yingchi Lu, Tingting Jiang, Jingsi Luo and Zailong Qin

   Content type:Case Report

   9 December 2019