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Results 1 - 10 of 289 for AA
  1. ... syndrome Dup(7)(q11.23) Somerville-Van der Aa syndrome Trisomy 7q11.23 WBS duplication syndrome Williams- ... or Free article on PubMed Central Van der Aa N, Rooms L, Vandeweyer G, van den Ende ...
  2. ... MyHC-beta myhc-slow MYHCB myosin heavy chain (AA 1-96) Myosin heavy chain 7 Myosin heavy ...
  3. ... This Health Condition alpha 1 (VI) chain (61 AA) CO6A1_HUMAN collagen alpha-1(VI) chain collagen ...
  4. ... More About This Health Condition ANT3_HUMAN antithrombin (aa 375-432) antithrombin III AT3 ATIII coding sequence ...
  5. ... to have family members with other autoimmune disorders. AA Alopecia circumscripta Genetic Testing Registry: Alopecia universalis Alopecia ...
  6. ... Citation on PubMed Makaryan V, Zeidler C, Bolyard AA, Skokowa J, Rodger E, Kelley ML, Boxer LA, ... BP, Link DC, Stein S, Rodger E, Bolyard AA, Aprikyan AA, Bonilla MA, Dror Y, Kannourakis G, ...
  7. ... intellectual disability-autism spectrum disorder Helsmoortel-van der Aa syndrome HVDAS Mental retardation, autosomal dominant 28 MRD28 ... Rare Disorders (NORD) ClinicalTrials.gov HELSMOORTEL-VAN DER AA SYNDROME; HVDAS PubMed Gozes I, Van Dijck A, ...
  8. ... 015. No abstract available. Citation on PubMed Bergen AA, Plomp AS, Schuurman EJ, Terry S, Breuning M, ... Leys A, Peek R, de Jong PT, Bergen AA. ABCC6/MRP6 mutations: further insight into the molecular ...
  9. ... BP, Link DC, Stein S, Rodger E, Bolyard AA, Aprikyan AA, Bonilla MA, Dror Y, Kannourakis G, Newburger PE, ... PubMed or Free article on PubMed Central Schaffer AA, Klein C. Genetic heterogeneity in severe congenital neutropenia: ...
  10. ... Leys A, Peek R, de Jong PT, Bergen AA. ABCC6/MRP6 mutations: further insight into the molecular ... D, Szeri F, Varadi A, Plomp A, Bergen AA, Oude Elferink RP, Borst P, van de Wetering ...
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