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Elucidating the genetic architecture of Adams–Oliver syndrome in a large European cohort - Meester - 2018 - Human Mutation - Wiley Online Library
The spectra of clinical phenotypes in aplasia cutis congenita and terminal transverse limb defects - Snape - 2009 - American Journal of Medical Genetics Part A - Wiley Online Library
Adams–Oliver Syndrome Type 2 in Association with Compound Heterozygous DOCK6 Mutations - Jones - 2017 - Pediatric Dermatology - Wiley Online Library
Another view of the newborn with Adams-Oliver syndrome associated with... | Download Scientific Diagram
Case report and review of literature of a rare congenital disorder: Adams-Oliver syndrome | BMC Anesthesiology | Full Text
Cornelia de Lange syndrome: MedlinePlus Genetics
Adams-Oliver syndrome: MedlinePlus Genetics
Adams-Oliver syndrome associated with gastrointestinal malformations | BMJ Case Reports
Adams–Oliver Syndrome Type 2 in Association with Compound Heterozygous DOCK6 Mutations - Jones - 2017 - Pediatric Dermatology - Wiley Online Library
Characteristic features of Adams–Oliver syndrome present in our set of... | Download Scientific Diagram
Adams Oliver syndrome: A mimicker of familial exudative vitreoretinopathy - ScienceDirect
Adams-Oliver syndrome: MedlinePlus Genetics
Syndrome d'Adams-Oliver et cutis marmorata telangiectatica congenita - ScienceDirect
Medicowesome: Medipicsowesome: Adams Oliver syndrome
Adams-Oliver syndrome: a case of bilateral progressive ischemic maculopathy - Journal of American Association for Pediatric Ophthalmology and Strabismus {JAAPOS}
Novel missense mutation in DLL4 in a Japanese sporadic case of Adams–Oliver syndrome | Journal of Human Genetics
Case report and review of literature of a rare congenital disorder: Adams-Oliver syndrome | BMC Anesthesiology | Full Text
The adult phenotype of Schaaf-Yang syndrome | Orphanet Journal of Rare Diseases | Full Text