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Paper Details

Adams-Oliver syndrome review of the literature: Refining the diagnostic phenotype.
Am J Med Genet A
55
2017
ACC, AOS, ARHGAP31, Adams-Oliver syndrome, CMTC, CNS anomalies, CNS migration defects, Cutis marmorata telangiectasia congenita, DLL4, DOCK6, EOGT, Hemorrhage, NOTCH1, RBPJ, TTLD, aplasia cutis congenita, central nervous system (CNS) anomalies, congenital heart defects, esophageal varices, hepatoportal sclerosis, microcephaly, portal hypertension, structural anomalies, transverse terminal limb defects, vascular anomalies, vascular defects, vascular sequelae
Author NameAffiliation
John J MulvihillUniversity of Oklahoma Health Sciences Center
John J MulvihillUniversity of Oklahoma Health Sciences Center
Christopher E AstonUniversity of Oklahoma Health Sciences Center
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Release 1.2