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Journal Abstract Search


155 related items for PubMed ID: 8673114

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  • 4. [Genetics in hypertension research. What can we learn from it regarding common essential hypertension?].
    Toka HR, Toka O, Luft FC.
    Fortschr Med; 1997 Oct 10; 115(28):36-8. PubMed ID: 9445830
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  • 5. Molecular genetics of the renin-angiotensin-aldosterone system in human hypertension.
    Corvol P, Soubrier F, Jeunemaitre X.
    Pathol Biol (Paris); 1997 Mar 10; 45(3):229-39. PubMed ID: 9296068
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  • 6. Autonomic nervous system function in patients with monogenic hypertension and brachydactyly: a field study in north-eastern Turkey.
    Tank J, Toka O, Toka HR, Jordan J, Diedrich A, Busjahn A, Luft FC.
    J Hum Hypertens; 2001 Nov 10; 15(11):787-92. PubMed ID: 11687923
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  • 7. [Monogenic hypertension].
    Bähr V, Oelkers W, Diederich S.
    Med Klin (Munich); 2003 Apr 15; 98(4):208-17. PubMed ID: 12715144
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  • 10. Refinement of the MYP3 locus on human chromosome 12 in a German family with Mendelian autosomal dominant high-grade myopia by SNP array mapping.
    Nürnberg G, Jacobi FK, Broghammer M, Becker C, Blin N, Nürnberg P, Stephani U, Pusch CM.
    Int J Mol Med; 2008 Apr 15; 21(4):429-38. PubMed ID: 18360688
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  • 11. A new form of autosomal dominant limb-girdle muscular dystrophy (LGMD1G) with progressive fingers and toes flexion limitation maps to chromosome 4p21.
    Starling A, Kok F, Passos-Bueno MR, Vainzof M, Zatz M.
    Eur J Hum Genet; 2004 Dec 15; 12(12):1033-40. PubMed ID: 15367920
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  • 17. Genome-wide linkage reveals a locus for human essential (primary) hypertension on chromosome 12p.
    Gong M, Zhang H, Schulz H, Lee YA, Sun K, Bähring S, Luft FC, Nürnberg P, Reis A, Rohde K, Ganten D, Hui R, Hübner N.
    Hum Mol Genet; 2003 Jun 01; 12(11):1273-7. PubMed ID: 12761042
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  • 18. Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21.
    Mansfield TA, Simon DB, Farfel Z, Bia M, Tucci JR, Lebel M, Gutkin M, Vialettes B, Christofilis MA, Kauppinen-Makelin R, Mayan H, Risch N, Lifton RP.
    Nat Genet; 1997 Jun 01; 16(2):202-5. PubMed ID: 9171836
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  • 20. Autosomal dominant hypertension and brachydactyly in a Turkish kindred resembles essential hypertension.
    Schuster H, Wienker TF, Toka HR, Bähring S, Jeschke E, Toka O, Busjahn A, Hempel A, Tahlhammer C, Oelkers W, Kunze J, Bilginturan N, Haller H, Luft FC.
    Hypertension; 1996 Dec 01; 28(6):1085-92. PubMed ID: 8952601
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