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

Por Li, Lin, Huang, Linhuan, Luo, Yanmin, Huang, Xuan, Lin, Shaobin, Fang, Qun
Publicado no Mol Syndromol (2016)

Clinical and molecular cytogenetic studies of an unrecognised 22q11.2 deletion in three families

Por HUANG, LINHUAN, XIE, YINGJUN, ZHOU, YI, LUO, YANMIN, HUANG, XUAN, XU, ZHE, CAI, DANLEI, FANG, QUN
Publicado no Exp Ther Med (2015)

FGFR3 gene mutation plus GRB10 gene duplication in a patient with achondroplasia plus growth delay with prenatal onset

Por Yuan, Haiming, Huang, Linhuan, Hu, Xizi, Li, Qian, Sun, Xiaofang, Xie, Yingjun, Kong, Shu, Wang, Xiaoman
Publicado no Orphanet J Rare Dis (2016)

Increased Expression and Altered Methylation of HERVWE1 in the Human Placentas of Smaller Fetuses from Monozygotic, Dichorionic, Discordant Twins

Por Gao, Yu, He, Zhiming, Wang, Zilian, Luo, Yanmin, Sun, Hongyu, Zhou, Yi, Huang, Linhuan, Li, Manchao, Fang, Qun, Jiang, Shiwen
Publicado em 2012