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Results 11 - 20 of 68 for Wilson sign
  1. Menkes syndrome 
    ... Lutsenko S. The copper-transporting ATPases, menkes and wilson disease proteins, have distinct roles in adult and ... P, Wijmenga C, Klomp LW. Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular ...
    https://medlineplus.gov/genetics/condition/menkes-syndrome - Genetics
  2. Cardiofaciocutaneous syndrome 
    ... Kutz W, Peck D, Rebolledo MA, Wheeler PG, Wilson W, Al-Rahawan MM, Stabley DL, Sol-Church ... Kavamura MI, Okamoto N, Kurosawa K, Hennekam RC, Wilson LC, Gillessen-Kaesbach G, Wieczorek D, Lapunzina P, ...
    https://medlineplus.gov/.../condition/cardiofaciocutaneous-syndrome - Genetics
  3. Nicolaides-Baraitser syndrome 
    ... N, Stolte-Dijkstra I, Verloes A, Wakeling E, Wilson L, Hennekam RC. Nicolaides-Baraitser syndrome: Delineation of ... Vilain C, Vogels A, Wakeling E, Wieczorek D, Wilson L, Zuffardi O, van Kampen AH, Devriendt K, ...
    https://medlineplus.gov/.../condition/nicolaides-baraitser-syndrome - Genetics
  4. CDKL5 deficiency disorder 
    ... 2016 Aug 16. Citation on PubMed Fehr S, Wilson M, Downs J, Williams S, Murgia A, Sartori ... Slean MM, Stephen E, Webb A, Vincent A, Wilson M. Incidence and phenotypes of childhood-onset genetic ...
    https://medlineplus.gov/genetics/condition/cdkl5-deficiency-disorder - Genetics
  5. Koolen-de Vries syndrome 
    ... Cuppen E, Baker C, Lee C, Graves TA, Wilson RK, Jenkins RB, Veltman JA, Eichler EE. Resolving ... Tan TY, Aftimos S, Worgan L, Susman R, Wilson M, Ghedia S, Kirk EP, Love D, Ronan ...
    https://medlineplus.gov/genetics/condition/koolen-de-vries-syndrome - Genetics
  6. Frontometaphyseal dysplasia 
    ... Superti-Furga A, Veenstra-Knol I, Wieczorek D, Wilson LC, Hennekam RC, Sutherland-Smith AJ, Strom TM, ... Superti-Furga A, Veenstra-Knol HE, Wieczorek D, Wilson LC, Markie DM, Robertson SP. Autosomal dominant frontometaphyseal ...
    https://medlineplus.gov/.../condition/frontometaphyseal-dysplasia - Genetics
  7. Abdominal wall defect 
    ... Citation on PubMed Mann S, Blinman TA, Douglas Wilson R. Prenatal and postnatal management of omphalocele. Prenat ... j.sempedsurg.2010.03.006. Citation on PubMed Wilson RD, Johnson MP. Congenital abdominal wall defects: an ...
    https://medlineplus.gov/genetics/condition/abdominal-wall-defect - Genetics
  8. Cantú syndrome 
    ... Lieshout S, Duran K, Renkens I, Amor DJ, Wilson LC, Kirk EP, Turner CL, Shears D, Garcia- ... 4):395-402. Citation on PubMed Scurr I, Wilson L, Lees M, Robertson S, Kirk E, Turner ...
    https://medlineplus.gov/genetics/condition/cantu-syndrome - Genetics
  9. Farsightedness 
    ... Bettecken T, Bencic G, Gieger C, Wichmann HE, Wilson JF, Venturini C, Fleck B, Cumberland PM, Rahi ... CC, Rotter JI, Pirastu M, Meitinger T, Bailey-Wilson JE, Stambolian D. Genome-wide meta-analysis of ...
    https://medlineplus.gov/genetics/condition/farsightedness - Genetics
  10. Pseudohypoaldosteronism type 2 
    ... on PubMed or Free article on PubMed Central Wilson FH, Disse-Nicodeme S, Choate KA, Ishikawa K, ... doi: 10.1126/science.1062844. Citation on PubMed Wilson FH, Kahle KT, Sabath E, Lalioti MD, Rapson ...
    https://medlineplus.gov/.../condition/pseudohypoaldosteronism-type-2 - Genetics
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