Dongzhi Li

发表

The Application of Crown‐Chin Length to Crown‐Rump Length Ratio in Predicting Fetal Skeletal Dysplasia at First Trimester

Xin Yang, Hang Zhou, Yingsi Li, 2022, Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine.

Prenatal Diagnosis of PPP2R1A-Related Neurodevelopmental Disorders Using Whole Exome Sequencing: Clinical Report and Review of Literature

C. Liao, T. Lei, F. Fu, 2023, Genes.

Case Report: Early diagnosis of lethal multiple pterygium syndrome with micrognathia: Two novel mutations in the CHRND gene

Ru Li, Xin Yang, Jin Han, 2023, Frontiers in Genetics.

Genetic Analysis and Sonography Characteristics in Fetus with SHOX Haploinsufficiency

C. Liao, F. Fu, Ru Li, 2023, Genes.

GATA zinc finger domain‐containing protein 2A (GATAD2A) deficiency reactivates fetal haemoglobin in patients with β‐thalassaemia through impaired formation of methyl‐binding domain protein 2 (MBD2)‐containing nucleosome remodelling and deacetylation (NuRD) complex

Dali Li, Yukio Nakamura, R. Kurita, 2021, British journal of haematology.

Whole exome sequencing improves genetic diagnosis of fetal clubfoot

C. Liao, T. Lei, F. Fu, 2022, Human Genetics.

Genetic diagnosis of fetal microcephaly at a single tertiary center in China

C. Liao, T. Lei, F. Fu, 2023, Frontiers in Genetics.

Identification of novel variations of oculocutaneous albinism type 2 with Prader–Willi syndrome/Angelman syndrome in two Chinese families

Jie Lei, Z. Fang, Hongyi Li, 2023, Frontiers in Genetics.

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

D. Liang, Zhuo Li, Lingqian Wu, 2023, Thrombosis and Haemostasis.

PDIA2 variant associated with vitiligo

C. Liao, Ru Li, X. Jing, 2023, Skin health and disease.

Utilization of multiple genetic methods for prenatal diagnosis of rare thalassemia variants

C. Liao, Jian Li, Fa-tao Li, 2023, Frontiers in genetics.

Prenatal diagnosis and early childhood outcome of fetuses with extremely large nuchal translucency

C. Liao, Xin Yang, M. Pan, 2023, Molecular Cytogenetics.

Exome sequencing improves genetic diagnosis of congenital orofacial clefts

C. Liao, T. Lei, F. Fu, 2023, Frontiers in genetics.

Should Prenatal Chromosomal Microarray Analysis Be Offered for Pulmonary Atresia? A Single-Center Retrospective Study in China

C. Liao, F. Fu, Ru Li, 2023, Genes.

Prenatal genetic diagnosis associated with fetal ventricular septal defect: an assessment based on chromosomal microarray analysis and exome sequencing

F. Fu, Ru Li, Ruibin Huang, 2023, Frontiers in genetics.

Chromosome Microarray Analysis and Exome Sequencing: Implementation in Prenatal Diagnosis of Fetuses with Digestive System Malformations

C. Liao, T. Lei, F. Fu, 2023, Genes.

Prenatal diagnosis in the fetal hyperechogenic kidneys: assessment using chromosomal microarray analysis and exome sequencing

C. Liao, T. Lei, F. Fu, 2023, Human Genetics.

Prenatal diagnosis and outcomes in fetuses with duplex kidney

F. Fu, Ru Li, Lushan Li, 2024, International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics.

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

F. Fu, Lushan Li, Ruibin Huang, 2024, Heliyon.

Implementation of high‐resolution SNP arrays in the investigation of fetuses with ultrasound malformations: 5 years of clinical experience

G. Xie, C. Liao, F. Fu, 2014, Clinical genetics.