Yingsi Li
Guangzhou, 510623, China
Last Updated: 09/26/2026
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Found 9 publications
Single-cell RNA sequencing reveals cellular and molecular landscape of fetal cystic hygroma.
Journal: BMC medical genomics
Published: June 27, 2023
Case report: A novel mosaic nonsense mutation of PCDH19 in a Chinese male with febrile epilepsy.
Journal: Frontiers in neurology
Published: July 13, 2022
Genetic causes of isolated and severe fetal growth restriction in normal chromosomal microarray analysis.
Journal: International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics
Published: June 19, 2022
Application of exome sequencing for prenatal diagnosis of fetal structural anomalies: clinical experience and lessons learned from a cohort of 1618 fetuses.
Journal: Genome medicine
Published: May 17, 2022
Prenatal diagnosis of Williams-Beuren syndrome by ultrasound and chromosomal microarray analysis.
Journal: Molecular cytogenetics
Published: March 28, 2022
The Genetic and Clinical Outcomes in Fetuses With Isolated Fetal Growth Restriction: A Chinese Single-Center Retrospective Study.
Journal: Frontiers in genetics
Published: January 17, 2022
Case Report: Two Novel L1CAM Mutations in Two Unrelated Chinese Families With X-Linked Hydrocephalus.
Journal: Frontiers in genetics
Published: November 08, 2021
The Application of Crown-Chin Length to Crown-Rump Length Ratio in Predicting Fetal Skeletal Dysplasia at First Trimester.
Journal: Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine
Published: September 01, 2021
Fetal Crown-Chin Length to Crown-Rump Length Ratio as a Prenatal Sonographic Marker for Triploidy at First Trimester.
Journal: Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine
Published: January 03, 2021
Showing 1-9 of 9
Last Updated: 09/26/2026