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Integrated CNV-seq, karyotyping and SNP-array analyses for effective prenatal diagnosis of chromosomal mosaicism
Integrated CNV-seq, karyotyping and SNP-array analyses for effective prenatal diagnosis of chromosomal mosaicism
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Integrated CNV-seq, karyotyping and SNP-array analyses for effective prenatal diagnosis of chromosomal mosaicism

Ma, Na ; Xi, Hui ; Chen, Jing ; Peng, Ying ; Jia, Zhengjun ; Yang, Shuting ; Hu, Jiancheng ; Pang, Jialun ; Zhang, Yanan ; Hu, Rong ; Wang, Hua ; Liu, Jing

BMC medical genomics, 2021-02, Vol.14 (1), p.56-56, Article 56 [Periódico revisado por pares]

England: BioMed Central Ltd

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2
Genome-wide copy number variant analysis for congenital ventricular septal defects in Chinese Han population
Genome-wide copy number variant analysis for congenital ventricular septal defects in Chinese Han population
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Genome-wide copy number variant analysis for congenital ventricular septal defects in Chinese Han population

An, Yu ; Duan, Wenyuan ; Huang, Guoying ; Chen, Xiaoli ; Li, Li ; Nie, Chenxia ; Hou, Jia ; Gui, Yonghao ; Wu, Yiming ; Zhang, Feng ; Shen, Yiping ; Wu, Bailin ; Wang, Hongyan

BMC medical genomics, 2016-01, Vol.9 (2), p.2-2, Article 2 [Periódico revisado por pares]

England: BioMed Central Ltd

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