Junhui Wan

Noninvasive prenatal testing of α-thalassemia and β-thalassemia through population-based parental haplotyping

Peixiang Ni, Zhiyu Peng, Jian Li, 2021, Genome medicine.

Association of an α-Globin Gene Cluster Duplication and Heterozygous β-Thalassemia in a Patient with a Severe Thalassemia Syndrome

Dongzhi Li, Ru Li, J. Wan, 2015, Hemoglobin.

Utilization of multiple genetic methods for prenatal diagnosis of rare thalassemia variants

C. Liao, Jian Li, Fa-tao Li, 2023, Frontiers in genetics.

Prenatal diagnosis of Smith-Magenis syndrome in two fetuses with increased nuchal translucency, mild lateral ventriculomegaly, and congenital heart defects.

C. Liao, T. Lei, F. Fu, 2016, Taiwanese journal of obstetrics & gynecology.

Detection of rare thalassemia mutations using long-read single-molecule real-time sequencing.

Feng Liu, Dongzhi Li, J. Wan, 2022, Gene.

Detection of fetal copy number variants by non‐invasive prenatal testing for common aneuploidies

C. Liao, Dongzhi Li, F. Fu, 2016, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Use of noninvasive prenatal screening with cell-free DNA in late pregnancy with sonographic soft markers.

Dongzhi Li, Xin Yang, L. Zhen, 2020, European journal of obstetrics, gynecology, and reproductive biology.

A novel splicing mutation of ARHGAP29 is associated with nonsyndromic cleft lip with or without cleft palate

Shaoqing Wu, C. Liao, Dongzhi Li, 2020, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.