• A heterozygous duplication variant of the HOXD13 gene caused synpolydactyly type 1 with variable expressivity in a Chinese family
• A Nonrandomized Trial of the Effects of Passive Simulated Jogging on Short-Term Heart Rate Variability in Type 2 Diabetic Subjects
• A Nonsense Mutation in HOXD13 Gene from A Chinese Family with Non-Syndromic Synpolydactyly
• A novel homozygous nonsense mutation in NECTIN4 gene in a Pakistani family with ectodermal dysplasia syndactyly syndrome 1
• A novel Hoxd13 mutation causes synpolydactyly and promotes osteoclast differentiation by regulating pSmad5/p65/c-Fos/Rank axis
• A novel microdeletion upstream of HOXD13 in a Chinese family with synpolydactyly
• A novel mutation of GLI3 gene underlying synpolydactyly in a family
• A Review of the Phenotype of Synpolydactyly Type 1 in Homozygous Patients: Defining the Relatively Long and Medially Deviated Big Toe with/without Cupping of the Forefoot as a Pathognomonic Feature in the Phenotype
• An Evolution of the Surgical Management of Synpolydactyly: A Case Series of 21 Hands
• An extremely rare case of Oro-facial digital syndrome: A case report
• Biallelic truncating variants in MAPKAPK5 cause a new developmental disorder involving neurological, cardiac, and facial anomalies combined with synpolydactyly
• Classification of synpolydactyly: experience in 10 children
• Current updates on arrhythmia within Timothy syndrome: genetics, mechanisms and therapeutics
• Deciphering the network of cholesterol biosynthesis in Paris polyphylla laid a base for efficient diosgenin production in plant chassis
• Exome sequencing identifies a novel nonsense mutation of HOXD13 in a Chinese family with synpolydactyly
• Exosome-mediated small interfering RNA delivery inhibits aberrant osteoblast differentiation in Apert syndrome model mice
• Homozygous <em>CHST11</em> mutation in chondrodysplasia, brachydactyly, overriding digits, clino-symphalangism and synpolydactyly
• HOXD13-associated synpolydactyly: Extending and validating the genotypic and phenotypic spectrum with 38 new and 49 published families
• 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
• Identification of broad, potent antibodies to functionally constrained regions of SARS-CoV-2 spike following a breakthrough infection
• Letter about a Published Paper
• Long-read whole genome sequencing reveals HOXD13 alterations in synpolydactyly
• Longitudinal outcomes for educational placement and quality of life in a prospectively recruited multinational cohort of children with cochlear implants
• 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
• Single-stage reconstruction of synpolydactyly: Our experience
• The changing epidemiology of syndactyly in Chinese newborns: a nationwide surveillance-based study
• Unblending of Transcriptional Condensates in Human Repeat Expansion Disease
• Validation of Knock-Out Caco-2 TC7 Cells as Models of Enterocytes of Patients with Familial Genetic Hypobetalipoproteinemias