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A rare mosaic 22q11.2 microdeletion identified in a Chinese family with recurrent fetal conotruncal defects 期刊论文
MOLECULAR GENETICS & GENOMIC MEDICINE, 2019, 卷号: 7, 期号: 8
作者:  Sheng, Wei;  Li, Xiaodi;  Sun, Liqun;  Huang, Guoying;  Chen, Weicheng
收藏  |  浏览/下载：18/0  |  提交时间：2019/12/05
Clinical application of chromosomal microarray analysis for the diagnosis of Williams–Beuren syndrome in Chinese Han patients 期刊论文
Molecular Genetics & Genomic Medicine, 2019, 卷号: Vol.7 No.2
作者:  Yu Xia;  Shufang Huang;  Yueheng Wu;  Yongchao Yang;  Shaoxian Chen
收藏  |  浏览/下载：24/0  |  提交时间：2019/12/13
Detection of copy number variants using chromosomal microarray analysis for the prenatal diagnosis of congenital heart defects with normal karyotype 期刊论文
JOURNAL OF CLINICAL LABORATORY ANALYSIS, 2019, 卷号: Vol.33 No.1
作者:  Song, Tingting;  Wan, Shanning;  Li, Yu;  Xu, Ying;  Dang, Yinghui
收藏  |  浏览/下载：40/0  |  提交时间：2019/12/17
Detection of 21q11.2-q22.11 deletions in a fetus by NIPT. 期刊论文
Journal of clinical laboratory analysis, 2019, 页码: e22711
作者:  Yunyun Zheng;  Biliang Chen;  Shanning Wan;  Hui Xu;  Yinghui Dang
收藏  |  浏览/下载：36/0  |  提交时间：2019/12/13
Detection of copy number variants using chromosomal microarray analysis for the prenatal diagnosis of congenital heart defects with normal karyotype 期刊论文
Journal of Clinical Laboratory Analysis, 2019, 卷号: Vol.33 No.1
作者:  Tingting Song;  Shanning Wan;  Yu Li;  Ying Xu;  Yinghui Dang
收藏  |  浏览/下载：25/0  |  提交时间：2019/12/13
Chromosomal microarray analysis in developmental delay and intellectual disability with comorbid conditions 期刊论文
BMC MEDICAL GENOMICS, 2018, 卷号: 11
作者:  Fan, Yanjie;  Wu, Yanming;  Wang, Lili;  Wang, Yu;  Gong, Zhuwen
收藏  |  浏览/下载：6/0  |  提交时间：2019/12/06
Upregulation of KIF20A correlates with poor prognosis in gastric cancer 期刊论文
CANCER MANAGEMENT AND RESEARCH, 2018, 卷号: 10, 页码: 6205-6216
作者:  Sheng, Yi;  Wang, Wei;  Hong, Bo;  Jiang, Xingwang;  Sun, Ruochuan
收藏  |  浏览/下载：23/0  |  提交时间：2019/12/25
[Clinical Application of Chromosomal Microarray Analysis in Karyotyping with Uncertain Genomic Rearrangement]. 期刊论文
Sichuan Da Xue Xue Bao Yi Xue Ban, 2017, 卷号: Vol.48 No.3, 页码: 460-463
作者:  Hu T;  Zhang Z;  Wang JM;  Liu HQ;  Liu ZY
收藏  |  浏览/下载：9/0  |  提交时间：2019/03/01
Performance evaluation of nipt in detection of chromosomal copy number variants using low-coverage whole-genome sequencing of plasma dna 期刊论文
Plos one, 2016, 卷号: 11, 期号: 7, 页码: 11
作者:  Liu, Hongtai;  Gao, Ya;  Hu, Zhiyang;  Lin, Linhua;  Yin, Xuyang
收藏  |  浏览/下载：38/0  |  提交时间：2019/05/09
Chromosomal microarray analysis in clinical evaluation of neurodevelopmental disorders-reporting a novel deletion of SETDB1 and illustration of counseling challenge 期刊论文
PEDIATRIC RESEARCH, 2016, 卷号: 80, 期号: 3
作者:  Xu, Qiong;  Goldstein, Jennifer;  Wang, Ping;  Gadi, Inder K.;  Labreche, Heather
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/05

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