GATA2 deficiency with early-onset interstitial pneumonia
Private Detection of Relatives in Forensic Genomics using Homomorphic Encryption
Evidence for a relationship between genetic polymorphisms of the L-DOPA transporter LAT2/4F2hc and risk of hypertension in the context of chronic kidney disease
Expression profile of urinary exosomal miRNAs in patients with diabetic kidney disease and their associated with kidney damage
Identification of a novel non-coding deletion in Allan-Herndon-Dudley syndrome by long-read HiFi genome sequencing
Causality between iron overload and osteoarthritis a Mendelian randomization study
Late-onset propionic acidemia with epilepsy due to compound heterozygous variants in the PCCB gene: a case report and literature review
Identification of a novel mutation of EYA4 in a Chinese family with delayed nonsyndromic hearing loss and analysis of molecular epidemiology of EYA4 mutations
Identifying inversions with Breakpoints in the Dystrophin Gene through Long-Read Sequencing: Report of Two Cases
Diverse cell death signature based subtypes predict the prognosis and immune characteristics within glioma