Evaluation of copy number variation detection for a SNP array platform

Por Zhang, Xin, Du, Renqian, Li, Shilin, Zhang, Feng, Jin, Li, Wang, Hongyan
Publicado em 2014

SIX2 haploinsufficiency causes conductive hearing loss with ptosis in humans

Por Guan, Jing, Wang, Dayong, Cao, Wenjian, Zhao, Yali, Du, Renqian, Yuan, Hu, Liu, Qiong, Lan, Lan, Zong, Liang, Yang, Ju, Yin, Zifang, Han, Bing, Zhang, Feng, Wang, Qiuju
Publicado no J Hum Genet (2016)

A Biallelic ANTXR1 Variant Expands the Anthrax Toxin Receptor Associated Phenotype to Tooth Agenesis

Por Dinckan, Nuriye, Du, Renqian, Akdemir, Zeynep Coban, Bayram, Yavuz, Jhiangiani, Shalini, Doddapaneni, Harsha, Hu, Jianhong, Muzny, Donna M., Guven, Yeliz, Aktoren, Oya, Kayserili, Hulya, Boerwinkle, Eric, Gibbs, Richard A., Posey, Jennifer E., Lupski, James R., Uyguner, Zehra Oya, Letra, Ariadne
Publicado no Am J Med Genet A (2018)