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Results 1 - 9 of 9 for "Adams-Oliver" syndrome 1
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  1. Adams-Oliver syndrome 
    ... Testing Registry: Adams-Oliver syndrome Genetic Testing Registry: Adams-Oliver syndrome 1 Genetic Testing Registry: Adams-Oliver syndrome 2 Genetic ... Oliver syndrome National Organization for Rare Disorders (NORD) ADAMS-OLIVER SYNDROME 1; AOS1 ADAMS-OLIVER SYNDROME 5; AOS5 ADAMS-OLIVER ...
    https://medlineplus.gov/genetics/condition/adams-oliver-syndrome - Genetics
  2. Nonsyndromic aplasia cutis congenita 
    ... in other conditions, including Johanson-Blizzard syndrome and Adams-Oliver syndrome. These instances are described as syndromic aplasia cutis congenita. Aplasia cutis congenita affects approximately 1 in 10,000 newborns. The incidence of the ...
    https://medlineplus.gov/.../nonsyndromic-aplasia-cutis-congenita - Genetics
  3. Bone Diseases (National Library of Medicine)  
    Your bones help you move, give you shape and support your body. They are living tissues that rebuild constantly throughout your life. During childhood and ...
    https://medlineplus.gov/bonediseases.html - Health Topics
  4. ARHGAP31 gene 
    ... limb reduction defects: extending the clinical spectrum of Adams-Oliver syndrome ... Rho GTPases lead the way. Dev Biol. 2004 Jan 1;265(1):23-32. doi: 10.1016/j. ...
    https://medlineplus.gov/genetics/gene/arhgap31 - Genetics
  5. NOTCH1 gene 
    The NOTCH1 gene provides instructions for making a protein called Notch1, a member of the Notch family of receptors. Receptor proteins have specific sites ...
    https://medlineplus.gov/genetics/gene/notch1 - Genetics
  6. RBPJ gene 
    ... by Notch signaling status. Genes Dev. 2013 May 1;27(9):1059-71. doi: ... families affected by Adams-Oliver syndrome. Am J Hum Genet. 2012 Aug 10;91( ...
    https://medlineplus.gov/genetics/gene/rbpj - Genetics
  7. DOCK6 gene 
    ... the way. Dev Biol. 2004 Jan 1;265(1):23-32. doi: 10.1016/j.ydbio.2003.06.003. ... organization and Adams-Oliver syndrome. Am J Hum Genet. 2011 Aug 12;89( ...
    https://medlineplus.gov/genetics/gene/dock6 - Genetics
  8. EOGT gene 
    ... EOGT gene have been found in individuals with Adams-Oliver syndrome. This condition is characterized by areas of missing ... or how it leads to the features of Adams-Oliver syndrome. More About This Health Condition AER61 AER61 glycosyltransferase ...
    https://medlineplus.gov/genetics/gene/eogt - Genetics
  9. Polymicrogyria 
    ... birth defects. These include 22q11.2 deletion syndrome, Adams-Oliver syndrome, Aicardi syndrome, Galloway-Mowat syndrome, Joubert syndrome, and ... Andermann F. Familial perisylvian polymicrogyria: a new familial syndrome of ... 2000 Jul;48(1):39-48. Citation on PubMed Guerrini R, Barkovich ...
    https://medlineplus.gov/genetics/condition/polymicrogyria - Genetics