Lingji T. Chen

18 Daoshan Road
Fuzhou, 350001, China

Last Updated: 09/26/2026

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Found 38 publications

Prenatally and postnatally sequential genetic etiology detection in corpus callosum abnormalities.

Prenatally and postnatally sequential genetic etiology detection in corpus callosum abnormalities.

Journal: Scientific reports
Published: February 27, 2025

Incidental finding of a DMD exons 48-55 deletion during prenatal diagnosis.

Incidental finding of a DMD exons 48-55 deletion during prenatal diagnosis.

Journal: Frontiers in pediatrics
Published: December 07, 2024

Congenital muscular dystrophies and myopathies: the leading cause of genetic muscular disorders in eleven Chinese families.

Congenital muscular dystrophies and myopathies: the leading cause of genetic muscular disorders in eleven Chinese families.

Journal: BMC musculoskeletal disorders
Published: November 12, 2024

Prenatal diagnosis of fetal skeletal anomalies via whole-exome sequencing in a tertiary referral center.

Prenatal diagnosis of fetal skeletal anomalies via whole-exome sequencing in a tertiary referral center.

Journal: Scientific reports
Published: February 01, 2024

Prenatal genetic diagnosis of fetuses with dextrocardia using whole exome sequencing in a tertiary center.

Prenatal genetic diagnosis of fetuses with dextrocardia using whole exome sequencing in a tertiary center.

Journal: Scientific reports
Published: January 31, 2024

First Report of Filipino β0-Thalassemia/β-Thalassemia in a Chinese Family.

First Report of Filipino β0-Thalassemia/β-Thalassemia in a Chinese Family.

Journal: Hemoglobin
Published: January 09, 2024

Fujian Province β-Thalassemia: A Molecular and Hematological Study in Southeastern China.

Fujian Province β-Thalassemia: A Molecular and Hematological Study in Southeastern China.

Journal: Genetics research
Published: November 14, 2023

Identification of a novel 91.5 kb-deletion (αα)FJ in the α-globin gene cluster using single-molecule real-time (SMRT) sequencing.

Identification of a novel 91.5 kb-deletion (αα)FJ in the α-globin gene cluster using single-molecule real-time (SMRT) sequencing.

Journal: The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians
Published: September 06, 2023

Mutation analysis of GJB2, SLC26A4, GJB3 and mtDNA12SrRNA genes in 251 non-syndromic hearing loss patients in Fujian, China.

Mutation analysis of GJB2, SLC26A4, GJB3 and mtDNA12SrRNA genes in 251 non-syndromic hearing loss patients in Fujian, China.

Journal: International journal of pediatric otorhinolaryngology
Published: July 25, 2023

Genetic testing for fetal loss of heterozygosity using single nucleotide polymorphism array and whole-exome sequencing.

Genetic testing for fetal loss of heterozygosity using single nucleotide polymorphism array and whole-exome sequencing.

Journal: Scientific reports
Published: July 03, 2023

The clinical value of hsa-miR-190b-5p in peripheral blood of pediatric β-thalassemia and its regulation on BCL11A expression.

The clinical value of hsa-miR-190b-5p in peripheral blood of pediatric β-thalassemia and its regulation on BCL11A expression.

Journal: PloS one
Published: April 18, 2023

Molecular genetic characteristics of a family which coinheritance of rare-88 C>G (HBB:c.-138 C>G) β-thalassemia mutation with α-thalassemia and review of the literature

Molecular genetic characteristics of a family which coinheritance of rare-88 C>G (HBB:c.-138 C>G) β-thalassemia mutation with α-thalassemia and review of the literature

Journal: Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine]
Published: February 16, 2023
Showing 1-12 of 38

Last Updated: 09/26/2026