Isolated chromosome 8p23.2-pter deletion: Novel evidence for developmental delay, intellectual disability, microcephaly and neurobehavioral disorders

von Shi, Shanshan, Lin, Shaobin, Chen, Baojiang, Zhou, Yi
Veröffentlicht in Mol Med Rep (2017)

Differing Microdeletion Sizes and Breakpoints in Chromosome 7q11.23 in Williams-Beuren Syndrome Detected by Chromosomal Microarray Analysis

von Li, Lin, Huang, Linhuan, Luo, Yanmin, Huang, Xuan, Lin, Shaobin, Fang, Qun
Veröffentlicht in Mol Syndromol (2016)

Prenatal diagnosis of Pallister‐Killian syndrome in one twin

von Li, Lin, Huang, Linhuan, Huang, Xuan, Lin, Shaobin, He, Zhiming, Fang, Qun
Veröffentlicht in Clin Case Rep (2018)

Clinical value of genetic analysis in prenatal diagnosis of short femur

von Liu, Jialiu, Huang, Linhuan, He, Zhiming, Lin, Shaobin, Wang, Ye, Luo, Yanmin
Veröffentlicht in Mol Genet Genomic Med (2019)

Chromosome 10q26 deletion syndrome: Two new cases and a review of the literature

von Lin, Shaobin, Zhou, Yi, Fang, Qun, Wu, Jianzhu, Zhang, Zhiqiang, Ji, Yuanjun, Luo, Yanmin
Veröffentlicht in Mol Med Rep (2016)

Individual heavy metal exposure and birth outcomes in Shenqiu county along the Huai River Basin in China

von Lin, Zhiqing, Chen, Xi, Xi, Zhuge, Lin, Shaobin, Sun, Xin, Jiang, Xiao, Tian, Haoyuan
Veröffentlicht in Toxicol Res (Camb) (2018)

Evaluation of a Microhaplotype-Based Noninvasive Prenatal Test in Twin Gestations: Determination of Paternity, Zygosity, and Fetal Fraction

von Bai, Zhaochen, Zhao, Hu, Lin, Shaobin, Huang, Linhuan, He, Zhiming, Wang, Huan, Ou, Xueling
Veröffentlicht in Genes (Basel) (2020)

Mosaic duplication of 8q24.1q24.3 detected by chromosomal microarray but not karyotyping in two unrelated fetuses with cardiac defects

von Lin, Shaobin, Huang, Shufang, Ou, Xueling, Gu, Heng, Wang, Yonghua, Li, Ping, Zhou, Yi
Veröffentlicht in Mol Cytogenet (2021)

Is an analysis of copy number variants necessary for various types of kidney ultrasound anomalies in fetuses?

von Lin, Shaobin, Shi, Shanshan, Huang, Linhuan, Lei, Ting, Cai, Danlei, Hu, Wenlong, Zhou, Yi, Luo, Yanmin
Veröffentlicht in Mol Cytogenet (2019)

A child with a novel DDX3X variant mimicking cerebral palsy: a case report

von Hu, Liqin, Xin, Xiaoqin, Lin, Shaobin, Luo, Min, Chen, Junkun, Qiu, Hongsheng, Ma, Li, Huang, Jungao
Veröffentlicht in Ital J Pediatr (2020)

A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature review

von Sha, Yanwei, Zheng, Liangkai, Ji, Zhiyong, Mei, Libin, Ding, Lu, Lin, Shaobin, Wang, Xu, Yang, Xiaoyu, Li, Ping
Veröffentlicht in BMC Med Genet (2018)

Case Report: Low-Level Maternal Mosaicism of a Novel CREBBP Variant Causes Recurrent Rubinstein-Taybi Syndrome in Two Siblings of a Chinese Family

von Lin, Shaobin, He, Zhiming, Huang, Linhuan, Liu, Jialiu, Lei, Ting, Wu, Jianzhu, Huang, Peizhi, Zhou, Yi, Luo, Yanmin
Veröffentlicht in Front Genet (2021)

EIF4G1 is a novel candidate gene associated with severe asthenozoospermia

von Sha, Yanwei, Liu, Wensheng, Huang, Xianjing, Li, Yang, Ji, Zhiyong, Mei, Libin, Lin, Shaobin, Kong, Shuangbo, Lu, Jinhua, Kong, Lingyuan, Zhu, Xingshen, Lu, Zhongxian, Ding, Lu
Veröffentlicht in Mol Genet Genomic Med (2019)

Higher blood cadmium level is associated with greater cognitive decline in rural Chinese adults aged 65 or older

von Liu, Hang, Su, Liqin, Chen, Xi, Wang, Sisi, Cheng, Yibin, Lin, Shaobin, Ding, Liang, Liu, Jingyi, Chen, Chen, Unverzagt, Frederick W, Hake, Ann M, Jin, Yinlong, Gao, Sujuan
Veröffentlicht in Sci Total Environ (2020)

Distributions of Heavy Metals in Maternal and Cord Blood and the Association with Infant Birth Weight in China

von Hu, Xiaobin, Zheng, Tongzhang, Cheng, Yibin, Holford, Theodore, Lin, Shaobin, Leaderer, Brian, Qiu, Jie, Bassig, Bryan A., Shi, Kunchong, Zhang, Yawei, Niu, Jianjun, Zhu, Yong, Li, Yonghong, Guo, Huan, Chen, Qiong, Zhang, Jianqing, Xu, Shunqing, Jin, Yinlong
Veröffentlicht in J Reprod Med (2015)

Prenatal exposure to organochlorine pesticides and infant birth weight in China

von Guo, Huan, Jin, Yinlong, Cheng, Yibin, Leaderer, Brian, Lin, Shaobin, Holford, Theodore R., Qiu, Jie, Zhang, Yawei, Shi, Kunchong, Zhu, Yong, Niu, Jianjun, Bassig, Bryan A., Xu, Shunqing, Zhang, Bin, Li, Yonghong, Hu, Xiaobin, Chen, Qiong, Zheng, Tongzhang
Veröffentlicht 2014

Cohort profile: China National Human Biomonitoring (CNHBM)—A nationally representative, prospective cohort in Chinese population

von Cao, Zhaojin, Lin, Shaobin, Zhao, Feng, Lv, Yuebin, Qu, Yingli, Hu, Xiaojian, Yu, Shicheng, Song, Shixun, Lu, Yifu, Yan, Huifang, Liu, Yingchun, Ding, Liang, Zhu, Ying, Liu, Ling, Zhang, Miao, Wang, Tong, Zhang, Wenli, Fu, Hui, Jin, Yongjin, Cai, Jiayi, Zhang, Xu, Yan, Chonghuai, Ji, Saisai, Zhang, Zhuona, Dai, Jiayin, Zhu, Huijuan, Gao, Lixue, Yang, Yanwei, Li, Chengcheng, Zhou, Jinhui, Ying, Bo, Zheng, Lei, Kang, Qi, Hu, Junming, Zhao, Weixia, Zhang, Mingyuan, Yu, Xiaoyi, Wu, Bing, Zheng, Tongzhang, Liu, Yang, Ryan, P. Barry, Barr, Dana Boyd, Qu, Weidong, Zheng, Yuxin, Shi, Xiaoming
Veröffentlicht in Environ Int (2020)