• A Cross-Sectional Study of the Neuropsychiatric Phenotype of CACNA1C-Related Disorder
• A novel homozygous nonsense mutation in NECTIN4 gene in a Pakistani family with ectodermal dysplasia syndactyly syndrome 1
• An Evolution of the Surgical Management of Synpolydactyly: A Case Series of 21 Hands
• Apert Syndrome Type III Hand: Prevalence and Outcomes
• Cardiac Behavior and Heart Rate Variability in Elderly Hypertensive Individuals during Aerobic Exercise: A Non-Randomized Controlled Study
• Correlation among Poincare plot and traditional heart rate variability indices in adults with different risk levels of metabolic syndrome: a cross-sectional approach from Southern India
• Deciphering the network of cholesterol biosynthesis in Paris polyphylla laid a base for efficient diosgenin production in plant chassis
• Dermatoglyphics in kidney diseases: a review
• Epidemiology of Congenital Upper-Limb Anomalies in Southern Taiwan Based on the Updated Oberg, Manske, and Tonkin Classification: A Series of 1,335 Anomalies in 1,188 Patients
• Exosome-mediated small interfering RNA delivery inhibits aberrant osteoblast differentiation in Apert syndrome model mice
• Heart Rate Variability Analysis May Identify Individuals With Williams-Beuren Syndrome at Risk of Sudden Death
• Identification of broad, potent antibodies to functionally constrained regions of SARS-CoV-2 spike following a breakthrough infection
• Mutations in HOXD13 underlie syndactyly type V and a novel brachydactyly-syndactyly syndrome
• Neurogenic hypertension characterizes children with congenital central hypoventilation syndrome and is aggravated by alveolar hypoventilation during sleep
• Organ Transplantation Outcomes of Deceased Organ Donors in Organ Procurement Organization-Based Recovery Facilities Versus Acute-Care Hospitals
• SURGICAL TREATMENT OF CONGENITAL TYPE V THUMB SYNDACTYLY
• Syndactyly type V
• The changing epidemiology of syndactyly in Chinese newborns: a nationwide surveillance-based study
• The pathogenic mechanism of syndactyly type V identified in a Hoxd13Q50R knock-in mice
• Validation of Knock-Out Caco-2 TC7 Cells as Models of Enterocytes of Patients with Familial Genetic Hypobetalipoproteinemias