Dong-zhi X. Li

Jinsui Road 9
Guangzhou, China

Last Updated: 09/26/2026

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Found 264 publications

Prenatal Diagnosis of PITX1-Related Limb Malformations in the Second Trimester.

Prenatal Diagnosis of PITX1-Related Limb Malformations in the Second Trimester.

Journal: Prenatal diagnosis
Published: April 12, 2026

Prenatal Diagnosis of White-Sutton Syndrome Associated With Autosomal Dominant POGZ Variants Presented With Craniofacial Abnormalities and Borderline Microcephaly Identified in the Second Trimester.

Prenatal Diagnosis of White-Sutton Syndrome Associated With Autosomal Dominant POGZ Variants Presented With Craniofacial Abnormalities and Borderline Microcephaly Identified in the Second Trimester.

Journal: Prenatal diagnosis
Published: April 02, 2026

Fetal Interrupted Aortic Arch and Unilateral Duplex Kidney Identified by Second Trimester Ultrasound Prompting Genetic Diagnosis of Neonatal Sclerosing Cholangitis.

Fetal Interrupted Aortic Arch and Unilateral Duplex Kidney Identified by Second Trimester Ultrasound Prompting Genetic Diagnosis of Neonatal Sclerosing Cholangitis.

Journal: Prenatal diagnosis
Published: April 02, 2026

Prenatal and molecular characteristics of 23 cases with Silver-Russell syndrome.

Prenatal and molecular characteristics of 23 cases with Silver-Russell syndrome.

Journal: Fetal diagnosis and therapy
Published: March 20, 2026

Prenatal sonographic features of Alagille syndrome: a single-center experience.

Prenatal sonographic features of Alagille syndrome: a single-center experience.

Journal: Fetal diagnosis and therapy
Published: March 17, 2026

Genetic Investigation of Fetal Left-Right Laterality Defects Identified in the Second Trimester of Pregnancy.

Genetic Investigation of Fetal Left-Right Laterality Defects Identified in the Second Trimester of Pregnancy.

Journal: Prenatal diagnosis
Published: March 03, 2026

Detecting Androgenetic Origin of the Genome via Single-Nucleotide Polymorphism-Based Cell-Free DNA Screening in Dichorionic Diamniotic Twin Pregnancies With Complete Hydatidiform Moles and a Coexisting Normal Fetus: A Three-Case Report.

Detecting Androgenetic Origin of the Genome via Single-Nucleotide Polymorphism-Based Cell-Free DNA Screening in Dichorionic Diamniotic Twin Pregnancies With Complete Hydatidiform Moles and a Coexisting Normal Fetus: A Three-Case Report.

Journal: Prenatal diagnosis
Published: March 02, 2026

Prenatal Diagnosis of Ververi-Brady Syndrome Associated With a Novel Nonsense QRICH1 Variant: A Case Presentation.

Prenatal Diagnosis of Ververi-Brady Syndrome Associated With a Novel Nonsense QRICH1 Variant: A Case Presentation.

Journal: Prenatal diagnosis
Published: February 27, 2026

Prenatal Diagnosis of Bachmann-Bupp Syndrome Associated With an ODC1 Variant Presented With Macrocephaly and Ventricular Septal Defect Identified by Second Trimester Ultrasound.

Prenatal Diagnosis of Bachmann-Bupp Syndrome Associated With an ODC1 Variant Presented With Macrocephaly and Ventricular Septal Defect Identified by Second Trimester Ultrasound.

Journal: Prenatal diagnosis
Published: February 11, 2026

Prenatal Diagnosis of CDK13-Related Disorder Presented With Isolated Polyhydramnios and Micrognathia.

Prenatal Diagnosis of CDK13-Related Disorder Presented With Isolated Polyhydramnios and Micrognathia.

Journal: Prenatal diagnosis
Published: December 17, 2025

Prenatal Diagnosis of Neurofibromatosis Type 1: No Specific Prenatal Features Observed in Sporadic Fetal Presentations.

Prenatal Diagnosis of Neurofibromatosis Type 1: No Specific Prenatal Features Observed in Sporadic Fetal Presentations.

Journal: Prenatal diagnosis
Published: December 04, 2025

Clinically Significant Genetic Results in Fetuses With Isolated Horseshoe Kidney.

Clinically Significant Genetic Results in Fetuses With Isolated Horseshoe Kidney.

Journal: Prenatal diagnosis
Published: October 26, 2025
Showing 1-12 of 264

Last Updated: 09/26/2026