• A de novo 2q35-q36.1 deletion incorporating IHH in a Chinese boy (47,XYY) with syndactyly, type III Waardenburg syndrome, and congenital heart disease
• An Evolution of the Surgical Management of Synpolydactyly: A Case Series of 21 Hands
• Apert Syndrome Type III Hand: Prevalence and Outcomes
• Congenital heart defects in oculodentodigital dysplasia: Report of two cases
• Deciphering the network of cholesterol biosynthesis in Paris polyphylla laid a base for efficient diosgenin production in plant chassis
• Genetic heterogeneity in type III familial cutaneous syndactyly and linkage to chromosome 7q36
• Heart Rate Variability Analysis May Identify Individuals With Williams-Beuren Syndrome at Risk of Sudden Death
• Identification of a Novel <em>IQCE</em> Large Deletion through Copy Number Variant Analysis from Whole-Exome Sequencing Data of a Patient with Postaxial Polydactyly Type A7
• Longitudinal outcomes for educational placement and quality of life in a prospectively recruited multinational cohort of children with cochlear implants
• Mathematical model presenting to assess variations in heart rate of ‎different age groups
• Oculodentodigital dysplasia with massive brain calcification and a new mutation of GJA1 gene
• Organ Transplantation Outcomes of Deceased Organ Donors in Organ Procurement Organization-Based Recovery Facilities Versus Acute-Care Hospitals
• Pfeiffer Syndrome
• Phenotypic Characterization of Timothy Syndrome Caused by the <em>CACNA1C</em> p.Gly402Ser Variant
• Probiotics of Lacticaseibacillus paracasei SD1 and Lacticaseibacillus rhamnosus SD11 attenuate inflammation and β-cell death in streptozotocin-induced type 1 diabetic mice
• Same Gene, Different Story (a Case Report of Congenital Long QT Syndrome Subtype 8 With a Novel Mutation)
• Syndactyly in the Pediatric Population: A Review of the Literature
• Syndactyly of the ring and little finger
• The changing epidemiology of syndactyly in Chinese newborns: a nationwide surveillance-based study
• Validation of Knock-Out Caco-2 TC7 Cells as Models of Enterocytes of Patients with Familial Genetic Hypobetalipoproteinemias