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Results 1 - 10 of 127 for aa
  1. 7q11.23 duplication syndrome 
    ... 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 ...
    https://medlineplus.gov/.../condition/7q1123-duplication-syndrome - Genetics
  2. Alopecia areata 
    ... to have family members with other autoimmune disorders. AA Alopecia circumscripta Genetic Testing Registry: Alopecia universalis Alopecia ...
    https://medlineplus.gov/genetics/condition/alopecia-areata - Genetics
  3. Severe congenital neutropenia 
    ... 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, ...
    https://medlineplus.gov/.../condition/severe-congenital-neutropenia - Genetics
  4. ADNP syndrome 
    ... 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, ...
    https://medlineplus.gov/genetics/condition/adnp-syndrome - Genetics
  5. Pseudoxanthoma elasticum 
    ... 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 ...
    https://medlineplus.gov/genetics/condition/pseudoxanthoma-elasticum - Genetics
  6. Catecholaminergic polymorphic ventricular tachycardia 
    ... PubMed Lieve KV, van der Werf C, Wilde AA. Catecholaminergic Polymorphic Ventricular Tachycardia. Circ J. 2016 May ... on PubMed Central van der Werf C, Wilde AA. Catecholaminergic polymorphic ventricular tachycardia: from bench to bedside. ...
    https://medlineplus.gov/...ergic-polymorphic-ventricular-tachycardia - Genetics
  7. Cone-rod dystrophy 
    ... Free article on PubMed Central Roosing S, Thiadens AA, Hoyng CB, Klaver CC, den Hollander AI, Cremers ... 1167/iovs.15-17604. Citation on PubMed Thiadens AA, Phan TM, Zekveld-Vroon RC, Leroy BP, van ...
    https://medlineplus.gov/genetics/condition/cone-rod-dystrophy - Genetics
  8. Progressive familial heart block 
    ... A, Baron E, Horie M, Hagiwara N, Wilde AA, Probst V, Le Marec H, Roden DM, Mochizuki ... F, Probst V, Hoorntje TM, Hulsbeek M, Wilde AA, Escande D, Mannens MM, Le Marec H. Cardiac ...
    https://medlineplus.gov/.../progressive-familial-heart-block - Genetics
  9. Complement component 2 deficiency 
    ... PubMed Jonsson G, Sjoholm AG, Truedsson L, Bengtsson AA, Braconier JH, Sturfelt G. Rheumatological manifestations, organ damage ... May 31. Citation on PubMed Truedsson L, Bengtsson AA, Sturfelt G. Complement deficiencies and systemic lupus erythematosus. ...
    https://medlineplus.gov/.../complement-component-2-deficiency - Genetics
  10. 15q13.3 microdeletion 
    ... Spiczak S, Kron KL, Steinich I, Kleefuss-Lie AA, Leu C, Gaus V, Schmitz B, Klein KM, ... Ounap K, Lachlan K, Castle B, Van der Aa N, van Ravenswaaij C, Nobrega MA, Serra-Juhe ...
    https://medlineplus.gov/genetics/condition/15q133-microdeletion - Genetics
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