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 *

49 related articles for article (PubMed ID: 6945804)

  • 1. Genetic linkage analysis of dermo-distortive urticaria.
    Epstein PA; Kidd KK; Sparkes RS
    Am J Med Genet; 1981; 9(4):317-21. PubMed ID: 6945804
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Dermo-distortive urticaria: an autosomal dominant dermatologic disorder.
    Epstein PA; Kidd KK
    Am J Med Genet; 1981; 9(4):307-15. PubMed ID: 7294069
    [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. The dopamine transporter protein gene (SLC6A3): primary linkage mapping and linkage studies in Tourette syndrome.
    Gelernter J; Vandenbergh D; Kruger SD; Pauls DL; Kurlan R; Pakstis AJ; Kidd KK; Uhl G
    Genomics; 1995 Dec; 30(3):459-63. PubMed ID: 8825631
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Integration of linkage analyses and disease association studies.
    Nemesure BB; He Q; Mendell N
    Genet Epidemiol; 1995; 12(6):653-8. PubMed ID: 8787989
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Familial idiopathic scoliosis: evidence of an X-linked susceptibility locus.
    Justice CM; Miller NH; Marosy B; Zhang J; Wilson AF
    Spine (Phila Pa 1976); 2003 Mar; 28(6):589-94. PubMed ID: 12642767
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Clinical phenotype and linkage analysis of the congenital fibrosis of the extraocular muscles in an Indian family.
    Venkatesh CP; Pillai VS; Raghunath A; Prakash VS; Vathsala R; Pericak-Vance MA; Kumar A
    Mol Vis; 2002 Aug; 8():294-7. PubMed ID: 12181522
    [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. [Clinical study and genetic 3q28 locus linkage in 2 Swiss families with Kjer dominant optic atrophy (OPA1)].
    Lefèvre A; Hiroz C; Zografos L; Schorderet DF; Munier FL
    Klin Monbl Augenheilkd; 1998 May; 212(5):301-4. PubMed ID: 9677562
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Genomewide survey of panic disorder.
    Crowe RR; Goedken R; Samuelson S; Wilson R; Nelson J; Noyes R
    Am J Med Genet; 2001 Jan; 105(1):105-9. PubMed ID: 11424978
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel candidate locus on chromosome 11p14.1-p11.2 for autosomal dominant hereditary spastic paraplegia.
    Zhao GH; Hu ZM; Shen L; Jiang H; Ren ZJ; Liu XM; Xia K; Guo P; Pan Q; Tang BS
    Chin Med J (Engl); 2008 Mar; 121(5):430-4. PubMed ID: 18364116
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Evaluation of linkage of markers on chromosome 6p with schizophrenia in Taiwanese families.
    Hwu HG; Lin MW; Lee PC; Lee SF; Ou-Yang WC; Liu CM
    Am J Med Genet; 2000 Feb; 96(1):74-8. PubMed ID: 10686556
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Linkage analysis with chromosome 9 markers in hereditary essential tremor.
    Conway D; Bain PG; Warner TT; Davis MB; Findley LJ; Thompson PD; Marsden CD; Harding AE
    Mov Disord; 1993 Jul; 8(3):374-6. PubMed ID: 8341306
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23.
    Bowles KR; Gajarski R; Porter P; Goytia V; Bachinski L; Roberts R; Pignatelli R; Towbin JA
    J Clin Invest; 1996 Sep; 98(6):1355-60. PubMed ID: 8823300
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel locus for generalized epilepsy with febrile seizures plus in French families.
    Baulac S; Gourfinkel-An I; Couarch P; Depienne C; Kaminska A; Dulac O; Baulac M; LeGuern E; Nabbout R
    Arch Neurol; 2008 Jul; 65(7):943-51. PubMed ID: 18625863
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Expanded genomewide scan implicates a novel locus at 3q28 among Caribbean hispanics with familial Alzheimer disease.
    Lee JH; Cheng R; Santana V; Williamson J; Lantigua R; Medrano M; Arriaga A; Stern Y; Tycko B; Rogaeva E; Wakutani Y; Kawarai T; St George-Hyslop P; Mayeux R
    Arch Neurol; 2006 Nov; 63(11):1591-8. PubMed ID: 17101828
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A new test statistic for linkage applied to bipolar disorder and marker D18S41.
    Cleves MA; Dawson DV; Elston RC; Schnell AH
    Genet Epidemiol; 1997; 14(6):581-6. PubMed ID: 9433546
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 3.