Caiqun Luo
Shenzhen, China
Last Updated: 09/26/2026
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Found 12 publications
Monochorionic dizygotic twins with discordant genetic findings and congenital malformations.
Journal: Clinical dysmorphology
Published: January 02, 2026
Amnioreduction as a therapeutic strategy for MAGED2 -related Bartter syndrome: prolonging gestation and improving outcomes through genetic-guided prenatal management.
Journal: Clinical dysmorphology
Published: July 14, 2025
CRISPR-Cas9-Generated TXNDC15 c.560delA Homozygous Mouse Model Exhibits Meckel-Gruber Syndrome Phenotype.
Journal: Genesis (New York, N.Y. : 2000)
Published: June 24, 2025
A Prenatal Ultrasound Study of Cerebral Cortical Sulci and Gyri Development in Fetuses With Overgrowth Syndrome and/or Cerebral Malformations due to Abnormalities in MTOR Pathway Genes.
Journal: Molecular genetics & genomic medicine
Published: May 09, 2025
The Utility of Whole Exome Sequencing in Fetuses With Isolated Increased Nuchal Translucency.
Journal: Molecular genetics & genomic medicine
Published: February 21, 2025
Autosomal recessive renal tubular dysgenesis: antenatal ultrasound scanning and molecular investigations.
Journal: Clinical dysmorphology
Published: December 06, 2024
Aberrant Fetal Brain Sulcus Formation: A Clue to the Diagnosis of Sotos Syndrome.
Journal: Prenatal diagnosis
Published: July 12, 2024
Application of Whole-Exome Sequencing in the Prenatal Diagnosis of Foetuses With Central Nervous System Abnormalities.
Journal: Molecular genetics & genomic medicine
Published: October 17, 2023
A Case Report and Literature Review of a Novel Mutation in the MAGED2 Gene of a Patient With Severe Transient Polyhydramnios.
Journal: Frontiers in pediatrics
Published: September 17, 2021
Circular RNA hsa_circ_0081343 promotes trophoblast cell migration and invasion and inhibits trophoblast apoptosis by regulating miR-210-5p/DLX3 axis.
Journal: Reproductive biology and endocrinology : RB&E
Published: March 23, 2021
UPD16 itself is not a cause of intrauterine growth restriction.
Journal: Fetal and pediatric pathology
Published: November 24, 2018
Genetic analysis and prenatal diagnosis for ten families affected with tuberous sclerosis complex
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: February 09, 2018
Showing 1-12 of 12
Last Updated: 09/26/2026