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 *

215 related articles for article (PubMed ID: 18463369)

  • 1. Autosomal dominant moyamoya disease maps to chromosome 17q25.3.
    Mineharu Y; Liu W; Inoue K; Matsuura N; Inoue S; Takenaka K; Ikeda H; Houkin K; Takagi Y; Kikuta K; Nozaki K; Hashimoto N; Koizumi A
    Neurology; 2008 Jun; 70(24 Pt 2):2357-63. PubMed ID: 18463369
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Autosomal dominant infantile gastroesophageal reflux disease: exclusion of a 13q14 locus in five well characterized families.
    Orenstein SR; Shalaby TM; Finch R; Pfuetzer RH; DeVandry S; Chensny LJ; Bannada MM; Whitcomb DC
    Am J Gastroenterol; 2002 Nov; 97(11):2725-32. PubMed ID: 12425539
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Genome-wide scan for myopia in the Old Order Amish.
    Stambolian D; Ciner EB; Reider LC; Moy C; Dana D; Owens R; Schlifka M; Holmes T; Ibay G; Bailey-Wilson JE
    Am J Ophthalmol; 2005 Sep; 140(3):469-76. PubMed ID: 16084785
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Further evidence of genetic heterogeneity segregating with hereditary gingival fibromatosis.
    Ye X; Shi L; Yin W; Meng L; Wang QK; Bian Z
    J Clin Periodontol; 2009 Aug; 36(8):627-33. PubMed ID: 19552635
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A narcolepsy susceptibility locus maps to a 5 Mb region of chromosome 21q.
    Dauvilliers Y; Blouin JL; Neidhart E; Carlander B; Eliaou JF; Antonarakis SE; Billiard M; Tafti M
    Ann Neurol; 2004 Sep; 56(3):382-8. PubMed ID: 15349865
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Evidence of a founder effect and refinement of the hereditary neuralgic amyotrophy (HNA) locus on 17q25 in American families.
    Watts GD; O'Briant KC; Chance PF
    Hum Genet; 2002 Feb; 110(2):166-72. PubMed ID: 11935323
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel gene locus for autosomal dominant left ventricular noncompaction maps to chromosome 11p15.
    Sasse-Klaassen S; Probst S; Gerull B; Oechslin E; Nürnberg P; Heuser A; Jenni R; Hennies HC; Thierfelder L
    Circulation; 2004 Jun; 109(22):2720-3. PubMed ID: 15173023
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Juvenile myoclonic epilepsy: linkage to chromosome 6p12 in Mexico families.
    Bai D; Alonso ME; Medina MT; Bailey JN; Morita R; Cordova S; Rasmussen A; Ramos-Peek J; Ochoa A; Jara A; Donnadieu FR; Cadena G; Yamakawa K; Delgado-Escueta AV
    Am J Med Genet; 2002 Dec; 113(3):268-74. PubMed ID: 12439895
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A genome screen of 35 bipolar affective disorder pedigrees provides significant evidence for a susceptibility locus on chromosome 15q25-26.
    McAuley EZ; Blair IP; Liu Z; Fullerton JM; Scimone A; Van Herten M; Evans MR; Kirkby KC; Donald JA; Mitchell PB; Schofield PR
    Mol Psychiatry; 2009 May; 14(5):492-500. PubMed ID: 18227837
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic refinement of the hereditary neuralgic amyotrophy (HNA) locus at chromosome 17q25.
    Meulemann J; Kuhlenbäumer G; Schirmacher A; Wehnert M; De Jonghe P; De Vriendt E; Young P; Airaksinen E; Pou-Serradell A; Prats JM; Ringelstein B; Stögbauer F; Van Broeckhoven C; Timmerman V
    Eur J Hum Genet; 1999 Dec; 7(8):920-7. PubMed ID: 10602368
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A genome-wide linkage scan in a Dutch family identifies a premature ovarian failure susceptibility locus.
    Oldenburg RA; van Dooren MF; de Graaf B; Simons E; Govaerts L; Swagemakers S; Verkerk JM; Oostra BA; Bertoli-Avella AM
    Hum Reprod; 2008 Dec; 23(12):2835-41. PubMed ID: 18689850
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mapping a new suggestive gene locus for autosomal dominant nephrolithiasis to chromosome 9q33.2-q34.2 by total genome search for linkage.
    Wolf MT; Zalewski I; Martin FC; Ruf R; Müller D; Hennies HC; Schwarz S; Panther F; Attanasio M; Acosta HG; Imm A; Lucke B; Utsch B; Otto E; Nurnberg P; Nieto VG; Hildebrandt F
    Nephrol Dial Transplant; 2005 May; 20(5):909-14. PubMed ID: 15741201
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Periodic catatonia: confirmation of linkage to chromosome 15 and further evidence for genetic heterogeneity.
    Stöber G; Seelow D; Rüschendorf F; Ekici A; Beckmann H; Reis A
    Hum Genet; 2002 Oct; 111(4-5):323-30. PubMed ID: 12384773
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia.
    Morita M; Al-Chalabi A; Andersen PM; Hosler B; Sapp P; Englund E; Mitchell JE; Habgood JJ; de Belleroche J; Xi J; Jongjaroenprasert W; Horvitz HR; Gunnarsson LG; Brown RH
    Neurology; 2006 Mar; 66(6):839-44. PubMed ID: 16421333
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Linkage of familial moyamoya disease (spontaneous occlusion of the circle of Willis) to chromosome 17q25.
    Yamauchi T; Tada M; Houkin K; Tanaka T; Nakamura Y; Kuroda S; Abe H; Inoue T; Ikezaki K; Matsushima T; Fukui M
    Stroke; 2000 Apr; 31(4):930-5. PubMed ID: 10754001
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Chromosome 10q harbors a susceptibility locus for bipolar disorder in Ashkenazi Jewish families.
    Venken T; Alaerts M; Souery D; Goossens D; Sluijs S; Navon R; Van Broeckhoven C; Mendlewicz J; Del-Favero J; Claes S
    Mol Psychiatry; 2008 Apr; 13(4):442-50. PubMed ID: 17579605
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Assignment of a locus for autosomal dominant idiopathic scoliosis (IS) to human chromosome 17p11.
    Salehi LB; Mangino M; De Serio S; De Cicco D; Capon F; Semprini S; Pizzuti A; Novelli G; Dallapiccola B
    Hum Genet; 2002 Oct; 111(4-5):401-4. PubMed ID: 12384783
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.