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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
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
Genetics of Autism Spectrum Disorders: The Opportunity and Challenge in the Genetics Clinic 图书章节
2015
作者:  Wang, Yi;  Wang, Ping;  Xu, Xiu;  Goldstein, Jennifer;  McConkie, Allyn
收藏  |  浏览/下载:6/0  |  提交时间:2019/12/19
Age- and gender-dependent obesity in individuals with 16p11.2 deletion 期刊论文
JOURNAL OF GENETICS AND GENOMICS, 2011, 卷号: 38, 期号: 9
作者:  Yu, Yongguo;  Zhu, Haitao;  Miller, David T.;  Gusella, James F.;  Platt, Orah S.
收藏  |  浏览/下载:2/0  |  提交时间:2019/12/19
Standardization and Diversification of Copy Number Microarray Testing for Clinical Diagnostics-Implications of the Cross-Platform/Algorithm Study on Clinical Diagnostic Chromosomal Microarray Analysis 期刊论文
CLINICAL CHEMISTRY, 2011, 卷号: 57, 期号: 10
作者:  Shen, Yiping;  An, Yu;  Wu, Bai-Lin
收藏  |  浏览/下载:2/0  |  提交时间:2019/12/19


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