Somatic Genomic Defects And Tumor Progression In NF1-associated Tumors
Performance of Cell-Free DNA Sequencing-Based Non-invasive Prenatal Testing: Our Experience on 36456 both Singleton and Multiple Pregnancies.
Whole-exome Sequencing Identify Rare Variants in Novel Candidate Genes with Non-syndromic Patent Ductus Arteriosus
Repeat to gene expression ratios in leukemic blast cells can stratify risk prediction in acute myeloid leukemia
Prenatal Methamphetamine Exposure could Cause Chronic Abnormalities in Transcriptomic Pattern; an Extended Follow-up Cohort Study
A novel synonymous ABCA3 variant identified in a Chinese family with lethal neonatal respiratory failure
Newborn Screening in Unselected Children Using Genomic Sequencing
Genome-wide Association Study Identifies New Loci Associated With Risk Of HBV Infection And Disease Progression
Familial SYN1 Pathogenic Mutations Related Neurodevelopmental Disorders in Asian Pediatric Patients
Integrated analysis of lncRNA-miRNA-mRNA ceRNA network and the potential prognosis indicators in sarcomas