Xie Yingjun
Guangdong Provincial Key Laboratory Of Major Obstetric Diseases
Guangzhou, China
Guangzhou, China
Last Updated: 09/26/2026
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Found 13 publications
The use of high-resolution SNP arrays to detect congenital cardiac defects.
Journal: 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
Published: February 04, 2024
Generation of two induced pluripotent stem cell lines, GZHMCi009-A and GZHMCi010-A, derived from peripheral blood mononuclear cells of two SCA3 patients with 14/74 CAG repeats of the ATXN3 mutation.
Journal: Stem cell research
Published: February 11, 2022
Epilepsy Combined With Multiple Gene Heterozygous Mutation.
Journal: Frontiers in pediatrics
Published: August 24, 2021
Generation of induced pluripotent stem cell GZHMCi001-A and GZHMCi001-B derived from peripheral blood mononuclear cells of epileptic patients with KCNC1 mutation.
Journal: Stem cell research
Published: May 14, 2020
Generation of four induced pluripotent stem cell lines, GZWWTi001-A, GZWTZi001-A, GZWXYi001-A, and GZWXDi001-A, derived from peripheral blood mononuclear cells from a family with asparagine synthetase deficiency.
Journal: Stem cell research
Published: August 01, 2019
CRISPR/Cas9 gene correction of HbH-CS thalassemia-induced pluripotent stem cells.
Journal: Annals of hematology
Published: January 20, 2019
Generation of GZKHQi001-A and GZWWTi001-A, two induced pluripotent stem cell lines derived from peripheral blood mononuclear cells of Duchenne muscular dystrophy patients.
Journal: Stem cell research
Published: October 22, 2017
Copy number variations independently induce autism spectrum disorder.
Journal: Bioscience reports
Published: December 05, 2016
Chromosomal uniparental disomy 16 and fetal intrauterine growth restriction.
Journal: European journal of obstetrics, gynecology, and reproductive biology
Published: October 28, 2016
Prader-Willi syndrome with a long-contiguous stretch of homozygosity not covering the critical region.
Journal: Journal of child neurology
Published: May 27, 2014
Microduplication of chromosome Xq25 encompassing STAG2 gene in a boy with intellectual disability.
Journal: European journal of medical genetics
Published: May 09, 2014
Last Updated: 09/26/2026