Shengfang Qin

Identification of an SRY-negative 46,XX infertility male with a heterozygous deletion downstream of SOX3 gene

Xueyan Wang, Shengfang Qin, Jin Wang, 2021, Molecular cytogenetics.

2+0 CYP21A2 deletion carrier — a limitation of the genetic testing and counseling: A case report

Xueyan Wang, Xi-min Chen, Shengfang Qin, 2021, World journal of clinical cases.

Verification of a cryptic t(Y;15) translocation in a male with an apparent 45,X karyotype

Yan Yin, J. Li-Ling, Mengling Ye, 2021, Molecular cytogenetics.

Growth hormone alleviates oxidative stress and improves the IVF outcomes of poor ovarian responders: a randomized controlled trial

D. Xiong, Jia-jing Wei, Yan Gong, 2020, Reproductive Biology and Endocrinology.

Growth hormone alleviates oxidative stress and improves IVF outcomes in Chinese women with poor ovarian response: A randomized controlled trial

D. Xiong, Jia-jing Wei, Yan Gong, 2020 .

Assessment of Combined Karyotype Analysis and Chromosome Microarray Analysis in Prenatal Diagnosis: A Cohort Study of 3710 Pregnancies

Mengling Ye, Zhu Zhang, Xueyan Wang, 2022, Genetics research.

Whole exome sequencing identifies c.963T > A and c.492 + 1G > A mutations in REN responsible for autosomal recessive renal tubular dysgenesis

J. Zhao, Xueyan Wang, Xi-min Chen, 2019, 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.

A novel SRY pathogenic variant from a 46,XY female harboring a nonsense point mutation (G to A) in position 293

Xueyan Wang, Shengfang Qin, Yunxing Li, 2021, Clinical case reports.