Ting Zhou

Prenatal diagnosis and molecular cytogenetic analyses of a paternal inherited deletion of 1q23.3 encompassing PBX1 gene

Man Luo, X. Gu, Ting Zhou, 2022, Molecular cytogenetics.

A rare case of uniparental isodisomy of chromosome 19 with no phenotypic abnormalities.

Bo Wang, Jieping Song, Ting Zhou, 2021, Taiwanese Journal of Obstetrics & Gynecology.