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Haploinsufficiency of the NOTCH1 Receptor as a Cause of Adams–Oliver Syndrome With Variable Cardiac Anomalies | Circulation: Cardiovascular Genetics
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Case report and review of literature of a rare congenital disorder: Adams-Oliver syndrome | BMC Anesthesiology | Full Text
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DOCK6 Mutations Are Responsible for a Distinct Autosomal‐Recessive Variant of Adams–Oliver Syndrome Associated with Brain and Eye Anomalies - Sukalo - 2015 - Human Mutation - Wiley Online Library
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John Libbey Eurotext - European Journal of Dermatology - Adams Oliver syndrome in association with neurological deficit
![A girl with Adams Oliver syndrome. She had terminal transverse limb... | Download Scientific Diagram A girl with Adams Oliver syndrome. She had terminal transverse limb... | Download Scientific Diagram](https://www.researchgate.net/publication/335444498/figure/fig13/AS:796823358799892@1566988901974/A-girl-with-Adams-Oliver-syndrome-She-had-terminal-transverse-limb-defects-hairless.png)
A girl with Adams Oliver syndrome. She had terminal transverse limb... | Download Scientific Diagram
MBBS students only - Adams Oliver Syndrome : 1. Absence defect of limbs, scalp and skull 2. Aplasia cutis congenita with Terminal transverse limb defects 3. Congenital scalp defects with Distal limb reduction anomalies.. | Facebook
![Management of large scalp and skull defects in a severe case of Adams-Oliver syndrome in: Journal of Neurosurgery: Pediatrics Volume 4 Issue 6 (2009) Journals Management of large scalp and skull defects in a severe case of Adams-Oliver syndrome in: Journal of Neurosurgery: Pediatrics Volume 4 Issue 6 (2009) Journals](https://thejns.org/pediatrics/view/journals/j-neurosurg-pediatr/4/6/0040523f1.jpg)
Management of large scalp and skull defects in a severe case of Adams-Oliver syndrome in: Journal of Neurosurgery: Pediatrics Volume 4 Issue 6 (2009) Journals
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Different Clinical Phenotypes in Adams-Oliver Syndrome Conservative Approach to Aplasia Cutis: A Report of Two Cases
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Novel missense mutation in DLL4 in a Japanese sporadic case of Adams–Oliver syndrome | Journal of Human Genetics
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