Fucheng Li

发表

The Genetic and Clinical Outcomes in Fetuses With Isolated Fetal Growth Restriction: A Chinese Single-Center Retrospective Study

C. Liao, Dongzhi Li, F. Fu, 2022, Frontiers in Genetics.

Prenatal exome sequencing in fetuses with congenital heart defects

C. Liao, Dongzhi Li, F. Fu, 2020, Clinical genetics.

Prenatal diagnosis of Williams-Beuren syndrome by ultrasound and chromosomal microarray analysis

C. Liao, Dongzhi Li, T. Lei, 2022, Molecular Cytogenetics.

A novel and a known mutation in LSS gene associated with hypotrichosis 14 in a Chinese family

C. Liao, Ru Li, X. Jing, 2019, The Journal of dermatology.

Prenatal diagnosis of 21 fetuses with balanced chromosomal abnormalities (BCAs) using whole-genome sequencing

C. Liao, Dongzhi Li, Weiyue Gu, 2022, Frontiers in Genetics.

Should prenatal chromosomal microarray analysis be offered for isolated ventricular septal defect? A single-center retrospective study from China

C. Liao, Dongzhi Li, T. Lei, 2022, Frontiers in Cardiovascular Medicine.

Application of exome sequencing for prenatal diagnosis of fetal structural anomalies: clinical experience and lessons learned from a cohort of 1618 fetuses

C. Liao, P. Fang, Dongzhi Li, 2022, Genome Medicine.

Characterization of 26 deletion CNVs reveals the frequent occurrence of micro-mutations within the breakpoint-flanking regions and frequent repair of double-strand breaks by templated insertions derived from remote genomic regions

Qibin Li, D. Cooper, C. Férec, 2015, Human Genetics.