Jiao Li

Guangxi Key Laboratory Of Birth Defects Research And Prevention, Guangxi Key Laboratory Of Reproductive Health And Birth Defects Prevention
Nanning, China

Last Updated: 09/26/2026

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Found 11 publications

NSF gene variants cause developmental and epileptic encephalopathy 96: expanding genotype and phenotypic spectrum with prenatal-onset features.

NSF gene variants cause developmental and epileptic encephalopathy 96: expanding genotype and phenotypic spectrum with prenatal-onset features.

Journal: Frontiers in genetics

Published: May 15, 2026

16p13.11 deletion/duplication: a large cohort study on prenatal diagnosis, postnatal outcomes, and phenotypic manifestations.

16p13.11 deletion/duplication: a large cohort study on prenatal diagnosis, postnatal outcomes, and phenotypic manifestations.

Journal: BMC pregnancy and childbirth

Published: July 06, 2025

Clinical and genetic profiles of postnatal patients with skeletal dysplasia in Guangxi during 8 years: a single-center experience.

Clinical and genetic profiles of postnatal patients with skeletal dysplasia in Guangxi during 8 years: a single-center experience.

Journal: Orphanet journal of rare diseases

Published: May 20, 2025

Catechol-grafted chitosan-based antioxidant hydrogel with rapid self-healing property for wound healing.

Catechol-grafted chitosan-based antioxidant hydrogel with rapid self-healing property for wound healing.

Journal: International journal of biological macromolecules

Published: September 11, 2024

Study of Mesoporous Zr-TiO2 Catalyst with Rich Oxygen Vacancies for N-Methylmorpholine Oxidation to N-Methylmorpholine-N-oxide.

Study of Mesoporous Zr-TiO2 Catalyst with Rich Oxygen Vacancies for N-Methylmorpholine Oxidation to N-Methylmorpholine-N-oxide.

Journal: Molecules (Basel, Switzerland)

Published: July 17, 2024

Structural enrichment and identification of lignin-carbohydrate complex in alkaline stabilized system.

Structural enrichment and identification of lignin-carbohydrate complex in alkaline stabilized system.

Journal: Carbohydrate polymers

Published: June 23, 2022

Compound variants of FKTN, POMGNT1, and LAMB1 gene identified by prenatal whole-exome sequencing in three fetuses with congenital hydrocephalus.

Compound variants of FKTN, POMGNT1, and LAMB1 gene identified by prenatal whole-exome sequencing in three fetuses with congenital hydrocephalus.

Journal: The journal of obstetrics and gynaecology research

Published: March 16, 2022

EGF signaling promotes the lineage conversion of astrocytes into oligodendrocytes.

EGF signaling promotes the lineage conversion of astrocytes into oligodendrocytes.

Journal: Molecular medicine (Cambridge, Mass.)

Published: January 09, 2022

Results of carrier screening and prenatal diagnosis for FMR1 gene in 819 cases

Results of carrier screening and prenatal diagnosis for FMR1 gene in 819 cases

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: September 14, 2020

Analyte-triggered autocatalytic amplification combined with gold nanoparticle probes for colorimetric detection of heavy-metal ions.

Analyte-triggered autocatalytic amplification combined with gold nanoparticle probes for colorimetric detection of heavy-metal ions.

Journal: Chemical communications (Cambridge, England)

Published: May 09, 2017

Application of single nucleotide polymorphism-array for the diagnosis of Williams-Beuren syndrome in a case

Application of single nucleotide polymorphism-array for the diagnosis of Williams-Beuren syndrome in a case

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: July 26, 2016

Showing 1-11 of 11

Last Updated: 09/26/2026