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

por Lin, Shaobin, Zhou, Yi, Fang, Qun, Wu, Jianzhu, Zhang, Zhiqiang, Ji, Yuanjun, Luo, Yanmin
Publicado 2016

EXT1 and EXT2 Variants in 22 Chinese Families With Multiple Osteochondromas: Seven New Variants and Potentiation of Preimplantation Genetic Testing and Prenatal Diagnosis

por Wang, Ye, Zhong, Liangying, Xu, Yan, Ding, Lei, Ji, Yuanjun, Schutz, Sacha, Férec, Claude, Cooper, David N., Xu, Caixia, Chen, Jian-Min, Luo, Yanmin
Publicado 2020