Q. Qin

SCHWANGERSCHAFTSPROTEIN 1 (SP1) AS A MATERNAL SERUM MARKER FOR DOWN SYNDROME IN THE FIRST AND SECOND TRIMESTERS

B. No̸rgaard-Pedersen, S. Larsen, M. Christiansen, 1997, Prenatal diagnosis.

FOXL2 gene mutations and blepharophimosis-ptosis-epicanthus inversus syndrome (BPES): a novel mutation detected in a Chinese family and a statistic model for summarizing previous reported records.

Liping Zhang, Yun-lian Zou, Xinmin Yan, 2009, Mutagenesis.