• A Drosophila Su(H) model of Adams-Oliver Syndrome reveals cofactor titration as a mechanism underlying developmental defects
• A novel pathogenic variation of DOCK6 gene: the genotype-phenotype correlation in Adams-Oliver syndrome
• Adams-Oliver Syndrome - A Case Report
• Adams-Oliver syndrome and associated complications: Report of a family in Colombia and review of the literature
• Adams-Oliver syndrome associated with refractory glaucoma
• Adams-Oliver syndrome: About a case
• Adams-Oliver Syndrome: Vestigial Tail and Genetics Update
• Atypical Adams-Oliver syndrome with typical ocular signs of familial exudative vitreoretinopathy
• Case report: Recombinant human epidermal growth factor gel plus kangfuxin solution in the treatment of aplasia cutis congenita in a case with Adams-Oliver syndrome
• Characterization of a New Variant in ARHGAP31 Probably Involved in Adams-Oliver Syndrome in a Family with a Variable Phenotypic Spectrum
• Cutaneous squamous cell carcinoma in an autosomal-recessive Adams-Oliver syndrome patient with a novel frameshift pathogenic variant in the EOGT gene
• Cutis marmorata telangiectatica congenita: Incidence of extracutaneous manifestations and a proposed clinical definition
• Encephalocele as a rare complication of conservatively managed cranial aplasia cutis in a boy with Adams-Oliver syndrome
• Expanding the phenotypic spectrum of NOTCH1 variants: clinical manifestations in families with congenital heart disease
• FOSL2 truncating variants in the last exon cause a neurodevelopmental disorder with scalp and enamel defects
• Heterozygous NOTCH1 Variants Cause CNS Immune Activation and Microangiopathy
• Human Genetics of Ventricular Septal Defect
• Intrafamilial phenotypic variability in autosomal recessive DOCK6-related Adams-Oliver syndrome
• NOTCH1 loss of the TAD and PEST domain: An antimorph?
• Synergistic effects of rare variants of ARHGAP31 and FBLN1 <em>in vitro</em> in terminal transverse limb defects
• The role of Notch signaling pathway in metabolic bone diseases