Lingping Li
Chengdu, China
Last Updated: 09/26/2026
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Found 9 publications
Evaluating the clinical utility and strategy of whole-exome sequencing testing for fetuses with increased nuchal translucency.
Journal: American journal of obstetrics and gynecology
Published: February 21, 2025
A prenatal case misunderstood as specimen confusion: 46,XY/46,XY chimerism.
Journal: BMC pregnancy and childbirth
Published: November 03, 2023
Unbalanced X;Y translocations carrying SRY in prenatal settings: Clinical, molecular, and cytogenetic analysis of three cases.
Journal: Prenatal diagnosis
Published: August 22, 2023
A chromosomal microarray analysis-based laboratory algorithm for the detection of genetic etiology of early pregnancy loss.
Journal: Frontiers in genetics
Published: April 11, 2023
Case report: Prenatal diagnosis of rare chromosome mosaicism: discordant results between chorionic villi and amniotic fluid samples.
Journal: Frontiers in genetics
Published: February 24, 2023
Clinical Selection of Prenatal Diagnostic Techniques Following Positive Noninvasive Prenatal Screening Results in Southwest China.
Journal: Frontiers in genetics
Published: November 08, 2021
Application of chromosomal microarray analysis in prenatal diagnosis for fetal abnormalities detected by ultrasonography
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: June 13, 2017
Application of chromosomal microarray analysis for the diagnosis of children with intellectual disability/developmental delay and a normal karytype
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: April 12, 2017
Showing 1-9 of 9
Last Updated: 09/26/2026