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 *

112 related articles for article (PubMed ID: 8320701)

  • 1. Linkage analysis of infantile pyloric stenosis and markers from chromosome 9q11-q33: no evidence for a major gene in this candidate region.
    Chung E; Coffey R; Parker K; Tam P; Pembrey ME; Gardiner RM
    J Med Genet; 1993 May; 30(5):393-5. PubMed ID: 8320701
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Preliminary linkage analysis of a Chinese family with benign familial infantile convulsion].
    Xiong G; Deng FY; Xiao B; Yang XS; Ning JC; Wu ZG; Wang K; Deng HW
    Zhonghua Er Ke Za Zhi; 2004 Jun; 42(6):424-8. PubMed ID: 15265426
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Linkage analysis of candidate regions in Swedish nonsyndromic cleft lip with or without cleft palate families.
    Wong FK; Hagberg C; Karsten A; Larson O; Gustavsson M; Huggare J; Larsson C; Teh BT; Linder-Aronson S
    Cleft Palate Craniofac J; 2000 Jul; 37(4):357-62. PubMed ID: 10912714
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Linkage of monogenic infantile hypertrophic pyloric stenosis to chromosome 16p12-p13 and evidence for genetic heterogeneity.
    Capon F; Reece A; Ravindrarajah R; Chung E
    Am J Hum Genet; 2006 Aug; 79(2):378-82. PubMed ID: 16826529
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Linkage of monogenic infantile hypertrophic pyloric stenosis to chromosome 16q24.
    Everett KV; Capon F; Georgoula C; Chioza BA; Reece A; Jaswon M; Pierro A; Puri P; Gardiner RM; Chung EM
    Eur J Hum Genet; 2008 Sep; 16(9):1151-4. PubMed ID: 18478043
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. A genome screen of a large bipolar affective disorder pedigree supports evidence for a susceptibility locus on chromosome 13q.
    Badenhop RF; Moses MJ; Scimone A; Mitchell PB; Ewen KR; Rosso A; Donald JA; Adams LJ; Schofield PR
    Mol Psychiatry; 2001 Jul; 6(4):396-403. PubMed ID: 11443523
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome.
    Winkelmann J; Lichtner P; Pütz B; Trenkwalder C; Hauk S; Meitinger T; Strom T; Muller-Myhsok B
    Mov Disord; 2006 Jan; 21(1):28-33. PubMed ID: 16124010
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Study of large inbred Friedreich ataxia families reveals a recombination between D9S15 and the disease locus.
    Belal S; Panayides K; Sirugo G; Ben Hamida C; Ioannou P; Hentati F; Beckmann J; Koenig M; Mandel JL; Ben Hamida M
    Am J Hum Genet; 1992 Dec; 51(6):1372-6. PubMed ID: 1463017
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic evidence for the neuronal nitric oxide synthase gene (NOS1) as a susceptibility locus for infantile pyloric stenosis.
    Chung E; Curtis D; Chen G; Marsden PA; Twells R; Xu W; Gardiner M
    Am J Hum Genet; 1996 Feb; 58(2):363-70. PubMed ID: 8571963
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A search for genes predisposing to manic depressive illness on chromosome 20.
    Ewald H; Eiberg H; Mors O
    Psychiatr Genet; 1995; 5(3):105-11. PubMed ID: 8746408
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A progressive autosomal recessive cataract locus maps to chromosome 9q13-q22.
    Héon E; Paterson AD; Fraser M; Billingsley G; Priston M; Balmer A; Schorderet DF; Verner A; Hudson TJ; Munier FL
    Am J Hum Genet; 2001 Mar; 68(3):772-7. PubMed ID: 11179024
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Scanning chromosome 17 for psoriasis susceptibility: lack of evidence for a distal 17q locus.
    Nair RP; Guo SW; Jenisch S; Henseler T; Lange EM; Terhune M; Westphal E; Christophers E; Voorhees JJ; Elder JT
    Hum Hered; 1995; 45(4):219-30. PubMed ID: 7558055
    [TBL] [Abstract][Full Text] [Related]  

  • 15. No evidence of linkage between manic depressive illness and the dopa decarboxylase gene or nearby region on chromosome 7p.
    Ewald H; Mors O; Eiberg H; Flint T; Kruse TA
    Psychiatr Genet; 1995; 5(4):161-9. PubMed ID: 8750358
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Determining trait locus position from multipoint analysis: accuracy and power of three different statistics.
    Greenberg DA; Abreu PC
    Genet Epidemiol; 2001 Dec; 21(4):299-314. PubMed ID: 11754466
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A new autosomal recessive retinitis pigmentosa locus maps on chromosome 2q31-q33.
    Bayés M; Goldaracena B; Martínez-Mir A; Iragui-Madoz MI; Solans T; Chivelet P; Bussaglia E; Ramos-Arroyo MA; Baiget M; Vilageliu L; Balcells S; Gonzàlez-Duarte R; Grinberg D
    J Med Genet; 1998 Feb; 35(2):141-5. PubMed ID: 9507394
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Linkage analysis of candidate genes in autoimmune thyroid disease. III. Detailed analysis of chromosome 14 localizes Graves' disease-1 (GD-1) close to multinodular goiter-1 (MNG-1). International Consortium for the Genetics of Autoimmune Thyroid Disease.
    Tomer Y; Barbesino G; Greenberg DA; Concepcion E; Davies TF
    J Clin Endocrinol Metab; 1998 Dec; 83(12):4321-7. PubMed ID: 9851771
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Digenic inheritance of an autosomal recessive hypotrichosis in two consanguineous pedigrees.
    Basit S; Wali A; Aziz A; Muhammad N; Jelani M; Ahmad W
    Clin Genet; 2011 Mar; 79(3):273-81. PubMed ID: 20528890
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.