Fucheng G. Li

No. 9 Jinsui Road, Tianhe District
Guangzhou, 510623, China

Last Updated: 09/26/2026

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Found 32 publications

Genetic architecture and prognostic significance of suspected fetal microcephaly: evidence from prenatal exome sequencing in a large prospective cohort.

Genetic architecture and prognostic significance of suspected fetal microcephaly: evidence from prenatal exome sequencing in a large prospective cohort.

Journal: Human genomics

Published: August 30, 2025

Genetic landscape and phenotypic correlations of lissencephaly: prenatal and postnatal insights.

Genetic landscape and phenotypic correlations of lissencephaly: prenatal and postnatal insights.

Journal: Brain communications

Published: July 10, 2025

Prenatal Exome Sequencing for Fetal Macrocephaly: A Large Prospective Observational Cohort Study.

Prenatal Exome Sequencing for Fetal Macrocephaly: A Large Prospective Observational Cohort Study.

Journal: Prenatal diagnosis

Published: February 12, 2025

Prenatal diagnosis of 17q12 copy number variants in fetuses via chromosomal microarray analysis - A retrospective cohort study and literature review.

Prenatal diagnosis of 17q12 copy number variants in fetuses via chromosomal microarray analysis - A retrospective cohort study and literature review.

Journal: Heliyon

Published: April 14, 2024

Association of prenatal Cleft Lip and Palate ultrasound abnormalities with copy number variants at a single Chinese tertiary center.

Association of prenatal Cleft Lip and Palate ultrasound abnormalities with copy number variants at a single Chinese tertiary center.

Journal: Italian journal of pediatrics

Published: January 07, 2024

Prenatal diagnosis and outcomes in fetuses with duplex kidney.

Prenatal diagnosis and outcomes in fetuses with duplex kidney.

Journal: International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics

Published: September 28, 2023

Prenatal diagnosis in fetal right aortic arch using chromosomal microarray analysis and whole exome sequencing: a Chinese single-center retrospective study.

Prenatal diagnosis in fetal right aortic arch using chromosomal microarray analysis and whole exome sequencing: a Chinese single-center retrospective study.

Journal: Molecular cytogenetics

Published: August 21, 2023

Prenatal diagnosis of polycystic renal diseases: diagnostic yield, novel disease-causing variants, and genotype-phenotype correlations.

Prenatal diagnosis of polycystic renal diseases: diagnostic yield, novel disease-causing variants, and genotype-phenotype correlations.

Journal: American journal of obstetrics & gynecology MFM

Published: August 06, 2023

Variant spectrum of F8 and F9 in hemophilia patients from southern China and 26 novel variants.

Variant spectrum of F8 and F9 in hemophilia patients from southern China and 26 novel variants.

Journal: Frontiers in genetics

Published: July 06, 2023

Exome sequencing improves genetic diagnosis of congenital orofacial clefts.

Exome sequencing improves genetic diagnosis of congenital orofacial clefts.

Journal: Frontiers in genetics

Published: July 04, 2023

Comprehensive Analysis of Hemophilia A (CAHEA): Towards Full Characterization of the F8 Gene Variants by Long-Read Sequencing.

Comprehensive Analysis of Hemophilia A (CAHEA): Towards Full Characterization of the F8 Gene Variants by Long-Read Sequencing.

Journal: Thrombosis and haemostasis

Published: June 07, 2023

Association of prenatal thoracic ultrasound abnormalities with copy number variants at a single Chinese tertiary center.

Association of prenatal thoracic ultrasound abnormalities with copy number variants at a single Chinese tertiary center.

Journal: International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics

Published: May 27, 2023

Showing 1-12 of 32

Last Updated: 09/26/2026