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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

69 related articles for article (PubMed ID: 19806567)

  • 1. [Linkage analysis of a family with familial hypertriglyceridemia].
    Tang X; Lin Y; Liu B; Ma S; Yang Y; Yang ZL
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Oct; 26(5):499-503. PubMed ID: 19806567
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.
    Lin MW; Lee DD; Lin CH; Huang CY; Wong CK; Chang YT; Liu HN; Hsiao KJ; Tsai SF
    Br J Dermatol; 2005 Jan; 152(1):29-36. PubMed ID: 15656797
    [TBL] [Abstract][Full Text] [Related]  

  • 3. CORD9 a new locus for arCRD: mapping to 8p11, estimation of frequency, evaluation of a candidate gene.
    Danciger M; Hendrickson J; Lyon J; Toomes C; McHale JC; Fishman GA; Inglehearn CF; Jacobson SG; Farber DB
    Invest Ophthalmol Vis Sci; 2001 Oct; 42(11):2458-65. PubMed ID: 11581183
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Localization of a gene for familial juvenile hyperuricemic nephropathy causing underexcretion-type gout to 16p12 by genome-wide linkage analysis of a large family.
    Kamatani N; Moritani M; Yamanaka H; Takeuchi F; Hosoya T; Itakura M
    Arthritis Rheum; 2000 Apr; 43(4):925-9. PubMed ID: 10765940
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Novel trabecular meshwork inducible glucocorticoid response mutation in an eight-generation juvenile-onset primary open-angle glaucoma pedigree.
    Richards JE; Ritch R; Lichter PR; Rozsa FW; Stringham HM; Caronia RM; Johnson D; Abundo GP; Willcockson J; Downs CA; Thompson DA; Musarella MA; Gupta N; Othman MI; Torrez DM; Herman SB; Wong DJ; Higashi M; Boehnke M
    Ophthalmology; 1998 Sep; 105(9):1698-707. PubMed ID: 9754180
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A genome-wide scan maps a novel juvenile-onset primary open-angle glaucoma locus to 15q.
    Wang DY; Fan BJ; Chua JK; Tam PO; Leung CK; Lam DS; Pang CP
    Invest Ophthalmol Vis Sci; 2006 Dec; 47(12):5315-21. PubMed ID: 17122119
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genes.
    McKay JD; Patterson B; Craig JE; Russell-Eggitt IM; Wirth MG; Burdon KP; Hewitt AW; Cohn AC; Kerdraon Y; Mackey DA
    Br J Ophthalmol; 2005 Jul; 89(7):831-4. PubMed ID: 15965161
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Evidence for a new locus for X-linked retinitis pigmentosa (RP23).
    Hardcastle AJ; Thiselton DL; Zito I; Ebenezer N; Mah TS; Gorin MB; Bhattacharya SS
    Invest Ophthalmol Vis Sci; 2000 Jul; 41(8):2080-6. PubMed ID: 10892847
    [TBL] [Abstract][Full Text] [Related]  

  • 9. First genomic localization of oculo-oto-dental syndrome with linkage to chromosome 20q13.1.
    Vieira H; Gregory-Evans K; Lim N; Brookes JL; Brueton LA; Gregory-Evans CY
    Invest Ophthalmol Vis Sci; 2002 Aug; 43(8):2540-5. PubMed ID: 12147582
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic linkage mapping for a susceptibility locus to bipolar illness: chromosomes 2, 3, 4, 7, 9, 10p, 11p, 22, and Xpter.
    Detera-Wadleigh SD; Hsieh WT; Berrettini WH; Goldin LR; Rollins DY; Muniec D; Grewal R; Guroff JJ; Turner G; Coffman D
    Am J Med Genet; 1994 Sep; 54(3):206-18. PubMed ID: 7810578
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Assignment of two loci for autosomal dominant adolescent idiopathic scoliosis to chromosomes 9q31.2-q34.2 and 17q25.3-qtel.
    Ocaka L; Zhao C; Reed JA; Ebenezer ND; Brice G; Morley T; Mehta M; O'Dowd J; Weber JL; Hardcastle AJ; Child AH
    J Med Genet; 2008 Feb; 45(2):87-92. PubMed ID: 17932119
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Exclusion of an extracolonic disease modifier locus on chromosome 1p33-36 in a large Swiss familial adenomatous polyposis kindred.
    Plasilova M; Russell AM; Wanner A; Wolf A; Dobbie Z; Müller HJ; Heinimann K
    Eur J Hum Genet; 2004 May; 12(5):365-71. PubMed ID: 14735163
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A genome-wide scan maps a novel juvenile-onset primary open angle glaucoma locus to chromosome 5q.
    Pang CP; Fan BJ; Canlas O; Wang DY; Dubois S; Tam PO; Lam DS; Raymond V; Ritch R
    Mol Vis; 2006 Feb; 12():85-92. PubMed ID: 16518310
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic linkage of snowflake vitreoretinal degeneration to chromosome 2q36.
    Jiao X; Ritter R; Hejtmancik JF; Edwards AO
    Invest Ophthalmol Vis Sci; 2004 Dec; 45(12):4498-503. PubMed ID: 15557460
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Evidence for linkage of restless legs syndrome to chromosome 9p: are there two distinct loci?
    Lohmann-Hedrich K; Neumann A; Kleensang A; Lohnau T; Muhle H; Djarmati A; König IR; Pramstaller PP; Schwinger E; Kramer PL; Ziegler A; Stephani U; Klein C
    Neurology; 2008 Feb; 70(9):686-94. PubMed ID: 18032746
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A new mutation in BFSP2 (G1091A) causes autosomal dominant congenital lamellar cataracts.
    Ma X; Li FF; Wang SZ; Gao C; Zhang M; Zhu SQ
    Mol Vis; 2008; 14():1906-11. PubMed ID: 18958306
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Linkage analysis of susceptibility genes for familial schizophrenia on chromosome 1 in Chinese population].
    Cai G; Wu X; Li T; Collier DA; Liu X; Feng B; Deng H; Tong D; Li J; Ou J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Dec; 19(6):491-4. PubMed ID: 12476422
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A new locus for inherited nuclear cataract mapped to the long arm of chromosome 1.
    Wang L; Lin H; Shen Y; Huang S; Gu J; Su H; Qi Y
    Mol Vis; 2007 Aug; 13():1357-62. PubMed ID: 17768382
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of a fourth locus (EVR4) for familial exudative vitreoretinopathy (FEVR).
    Toomes C; Downey LM; Bottomley HM; Scott S; Woodruff G; Trembath RC; Inglehearn CF
    Mol Vis; 2004 Jan; 10():37-42. PubMed ID: 14737064
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical description and genome wide linkage study of Y-sutural cataract and myopia in a Chinese family.
    Zhang Q; Guo X; Xiao X; Yi J; Jia X; Hejtmancik JF
    Mol Vis; 2004 Nov; 10():890-900. PubMed ID: 15570218
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.