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Results 1 - 10 of 1,091 for R -CR8
  1. Laron syndrome 
    ... person has one parent with the condition. GH-R deficiency Growth hormone insensitivity syndrome Growth hormone receptor ... Montalvo A, Saavedra J, Ingles S, de Cabo R, Cohen P, Longo VD. Growth hormone receptor deficiency ...
    https://medlineplus.gov/genetics/condition/laron-syndrome - Genetics
  2. Ulcerative colitis 
    ... P, Imielinski M, Latiano A, Lagace C, Scott R, Amininejad L, Bumpstead S, Baidoo L, Baldassano RN, ... M, Dubinsky M, Edwards C, Ellinghaus D, Fehrmann RS, Floyd JA, Florin T, Franchimont D, Franke L, ...
    https://medlineplus.gov/genetics/condition/ulcerative-colitis - Genetics
  3. Type 2 diabetes 
    ... A, Been LF, Beilby J, Bell GI, Benediktsson R, Bergman RN, Boehm BO, Boerwinkle E, Bonnycastle LL, ... J, Edkins S, Elliott P, Emilsson V, Erbel R, Eriksson JG, Escobedo J, Esko T, Eury E, ...
    https://medlineplus.gov/genetics/condition/type-2-diabetes - Genetics
  4. GRN-related frontotemporal lobar degeneration 
    ... D, Dheel C, Fields J, Forsberg L, Gavrilova R, Gearhart D, Graff-Radford J, Graff-Radford N, ... D, Knopman D, Kremers WK, Lapid M, Rademakers R, Ramos EM, Syrjanen J, Boxer AL, Rosen H, ...
    https://medlineplus.gov/...related-frontotemporal-lobar-degeneration - Genetics
  5. Trisomy 18 
    ... NORD) ClinicalTrials.gov PubMed Boghosian-Sell L, Mewar R, Harrison W, Shapiro RM, Zackai EH, Carey J, ... PubMed or Free article on PubMed Central Bronsteen R, Lee W, Vettraino IM, Huang R, Comstock CH. ...
    https://medlineplus.gov/genetics/condition/trisomy-18 - Genetics
  6. Aicardi-Goutières syndrome 
    ... Arellano M, Ariaudo G, Aswani V, Babul-Hirji R, Baildam EM, Bahi-Buisson N, Bailey KM, Barnerias C, Barth M, Battini R, Beresford MW, Bernard G, Bianchi M, Billette de ...
    https://medlineplus.gov/.../condition/aicardi-goutieres-syndrome - Genetics
  7. Autosomal dominant epilepsy with auditory features 
    ... A, Giallonardo AT, Mecarelli O, Tosatto SC, Ottman R, Michelucci R, Nobile C. Heterozygous reelin mutations cause autosomal-dominant ... Citation on PubMed Dazzo E, Rehberg K, Michelucci R, Passarelli D, Boniver C, Vianello Dri V, Striano ...
    https://medlineplus.gov/...-dominant-epilepsy-with-auditory-features - Genetics
  8. Ehlers-Danlos syndrome 
    ... C, Kapferer-Seebacher I, Kosho T, Mendoza-Londono R, Pope MF, Rohrbach M, Van Damme T, Vandersteen ... Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews(R) [Internet]. Seattle (WA): University of Washington, Seattle; 1993- ...
    https://medlineplus.gov/genetics/condition/ehlers-danlos-syndrome -
  9. Hereditary diffuse gastric cancer 
    ... F, Figueiredo C, Paredes J, Oliveira C, Seruca R. E-cadherin dysfunction in gastric cancer--cellular consequences, ... Simoes-Correia J, Grannas K, Suriano G, Seruca R. The importance of E-cadherin binding partners to ...
    https://medlineplus.gov/.../hereditary-diffuse-gastric-cancer - Genetics
  10. Lynch syndrome 
    ... N, Katz LH, Heinimann K, Vaccaro CA, Buttner R, Gorgens H, Holinski-Feder E, Morak M, Holzapfel S, Huneburg R, Knebel Doeberitz MV, Loeffler M, Rahner N, Schackert ...
    https://medlineplus.gov/genetics/condition/lynch-syndrome - Genetics
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