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Adams Oliver syndrome

  1. [Management of congenital scalp defects in infants].
  2. Recessive Mutations in DOCK6, Encoding the Guanidine Nucleotide Exchange Factor DOCK6, Lead to Abnormal Actin Cytoskeleton Organization and Adams-Oliver Syndrome.
  3. Adams-Oliver syndrome, a family with dominant inheritance and a severe phenotype.
  4. [Adams-Oliver syndrome: case report].
  5. Autosomal dominant aplasia cutis in three generations and one case with preaxial polydactyly in the last generation.
  6. Adams-Oliver syndrome associated with bilateral anterior polar cataracts and optic disk drusen.
  7. Gain-of-Function Mutations of ARHGAP31, a Cdc42/Rac1 GTPase Regulator, Cause Syndromic Cutis Aplasia and Limb Anomalies.
  8. [Cutis verticis gyrata with a combined blue and congenital dermal nevus].
  9. Herniation of the brain after conservative treatment of a large congenital skull defect in an infant with Adams-Oliver syndrome.
  10. [The Adams-Oliver syndrome. A case report.]
  11. [Adams-Oliver syndrome: A case with minimal expression.]
  12. A case of adams-oliver syndrome.
  13. Periventricular nodular heterotopia and distal limb deficiency: a recurrent association.
  14. Adams Oliver syndrome in association with neurological deficit.
  15. Management of large scalp and skull defects in a severe case of Adams-Oliver syndrome.
  16. The relationship between acquired impairments of executive function and behaviour change in adults with Down syndrome.
  17. Do children with Adams-Oliver syndrome require endocrine follow-up? New information on the phenotype and management.
  18. Adams-Oliver syndrome: Additions to the clinical features and possible role of BMP pathway.
  19. The spectra of clinical phenotypes in aplasia cutis congenita and terminal transverse limb defects.
  20. Aplasia cutis congenita, terminal limb defects and periventricular leukomalacia in one sibling with minor findings in the other-probable autosomal recessive Adams-Oliver Syndrome.