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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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Autosomal recessive Adams–Oliver syndrome caused by homozygous mutation in EOGT, encoding an EGF domain-specific O-GlcNAc transferase | European Journal of Human Genetics
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
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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
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