Mild Cornelia De Lange Syndrome
Dec. 23, 2024
Figure 1 from Two novel RAD21 mutations in patients with mild Cornelia de Lange syndrome-like presentation and report of the first familial case. | Semantic Scholar Genes | Free Full-Text | Cornelia de Lange Syndrome: From a Disease to a Broader Spectrum Representative facies in mild NIPBL and SMC1A-mutated CdLS patients.... | Download Scientific Diagram Overview of the phenotype and molecular findings of two patients with... | Download Scientific Diagram Cornelia de Lange syndrome causes, symptoms, prognosis and treatment Isolated NIBPL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction | European Journal of Human Genetics | Mild Cornelia De Lange Syndrome