These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

99 related items for PubMed ID: 12761042

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Severe autosomal dominant hypertension and brachydactyly in a unique Turkish kindred maps to human chromosome 12.
    Schuster H, Wienker TE, Bähring S, Bilginturan N, Toka HR, Neitzel H, Jeschke E, Toka O, Gilbert D, Lowe A, Ott J, Haller H, Luft FC.
    Nat Genet; 1996 May 01; 13(1):98-100. PubMed ID: 8673114
    [Abstract] [Full Text] [Related]

  • 3. Genome-wide linkage analysis of severe, early-onset chronic obstructive pulmonary disease: airflow obstruction and chronic bronchitis phenotypes.
    Silverman EK, Mosley JD, Palmer LJ, Barth M, Senter JM, Brown A, Drazen JM, Kwiatkowski DJ, Chapman HA, Campbell EJ, Province MA, Rao DC, Reilly JJ, Ginns LC, Speizer FE, Weiss ST.
    Hum Mol Genet; 2002 Mar 15; 11(6):623-32. PubMed ID: 11912177
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Families with autosomal dominant brachydactyly type E, short stature, and severe hypertension.
    Toka HR, Bähring S, Chitayat D, Melby JC, Whitehead R, Jeschke E, Wienker TF, Toka O, Schuster H, Luft FC.
    Ann Intern Med; 1998 Aug 01; 129(3):204-8. PubMed ID: 9696728
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Genome-wide linkage analysis reveals evidence for four new susceptibility loci for familial euthyroid goiter.
    Bayer Y, Neumann S, Meyer B, Rüschendorf F, Reske A, Brix T, Hegedüs L, Langer P, Nürnberg P, Paschke R.
    J Clin Endocrinol Metab; 2004 Aug 01; 89(8):4044-52. PubMed ID: 15292347
    [Abstract] [Full Text] [Related]

  • 9. Fine mapping of 10q and 18q for familial Alzheimer's disease in Caribbean Hispanics.
    Lee JH, Mayeux R, Mayo D, Mo J, Santana V, Williamson J, Flaquer A, Ciappa A, Rondon H, Estevez P, Lantigua R, Kawarai T, Toulina A, Medrano M, Torres M, Stern Y, Tycko B, Rogaeva E, St George-Hyslop P, Knowles JA.
    Mol Psychiatry; 2004 Nov 01; 9(11):1042-51. PubMed ID: 15241431
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Genetic susceptibility loci for essential hypertension and blood pressure on chromosome 17 in 147 Chinese pedigrees.
    Gu F, Ge D, Huang J, Chen J, Yang W, Gu D.
    J Hypertens; 2004 Aug 01; 22(8):1511-8. PubMed ID: 15257173
    [Abstract] [Full Text] [Related]

  • 13. A genome-wide scan shows significant linkage between bipolar disorder and chromosome 12q24.3 and suggestive linkage to chromosomes 1p22-21, 4p16, 6q14-22, 10q26 and 16p13.3.
    Ewald H, Flint T, Kruse TA, Mors O.
    Mol Psychiatry; 2002 Aug 01; 7(7):734-44. PubMed ID: 12192618
    [Abstract] [Full Text] [Related]

  • 14. A genome scan for hypertension susceptibility loci in populations of Chinese and Japanese origins.
    Ranade K, Hinds D, Hsiung CA, Chuang LM, Chang MS, Chen YT, Pesich R, Hebert J, Chen YD, Dzau V, Olshen R, Curb D, Botstein D, Cox DR, Risch N.
    Am J Hypertens; 2003 Feb 01; 16(2):158-62. PubMed ID: 12559686
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. New susceptibility locus for hypertension on chromosome 8q by efficient pedigree-breaking in an Italian isolate.
    Ciullo M, Bellenguez C, Colonna V, Nutile T, Calabria A, Pacente R, Iovino G, Trimarco B, Bourgain C, Persico MG.
    Hum Mol Genet; 2006 May 15; 15(10):1735-43. PubMed ID: 16611673
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 5.