Disease: Syndactyly- type 2
- 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