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 *

136 related articles for article (PubMed ID: 8579335)

  • 1. An extension of the Maximum Lod Score method to X-linked loci.
    Cordell HJ; Kawaguchi Y; Todd JA; Farrall M
    Ann Hum Genet; 1995 Oct; 59(4):435-49. PubMed ID: 8579335
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Two-locus maximum lod score analysis of a multifactorial trait: joint consideration of IDDM2 and IDDM4 with IDDM1 in type 1 diabetes.
    Cordell HJ; Todd JA; Bennett ST; Kawaguchi Y; Farrall M
    Am J Hum Genet; 1995 Oct; 57(4):920-34. PubMed ID: 7573054
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Multilocus linkage tests based on affected relative pairs.
    Cordell HJ; Wedig GC; Jacobs KB; Elston RC
    Am J Hum Genet; 2000 Apr; 66(4):1273-86. PubMed ID: 10729111
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Asymptotic properties of affected-sib-pair linkage analysis.
    Holmans P
    Am J Hum Genet; 1993 Feb; 52(2):362-74. PubMed ID: 8430697
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Linkage analysis of a large pedigree with hereditary sideroblastic anaemia.
    Noble JS; Taylor GR; Losowsky MS; Hall R; Turner G; Mueller RF; Stewart AD
    J Med Genet; 1995 May; 32(5):389-92. PubMed ID: 7616548
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A general conditional-logistic model for affected-relative-pair linkage studies.
    Olson JM
    Am J Hum Genet; 1999 Dec; 65(6):1760-9. PubMed ID: 10577930
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel X-linked dominant condition: X-linked congenital isolated ptosis.
    McMullan TF; Collins AR; Tyers AG; Robinson DO
    Am J Hum Genet; 2000 Apr; 66(4):1455-60. PubMed ID: 10739771
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Estimating the power of a proposed linkage study: a practical computer simulation approach.
    Boehnke M
    Am J Hum Genet; 1986 Oct; 39(4):513-27. PubMed ID: 3464203
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Two-locus models of disease: comparison of likelihood and nonparametric linkage methods.
    Goldin LR; Weeks DE
    Am J Hum Genet; 1993 Oct; 53(4):908-15. PubMed ID: 8213819
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Complete genomic screen in late-onset familial Alzheimer disease. Evidence for a new locus on chromosome 12.
    Pericak-Vance MA; Bass MP; Yamaoka LH; Gaskell PC; Scott WK; Terwedow HA; Menold MM; Conneally PM; Small GW; Vance JM; Saunders AM; Roses AD; Haines JL
    JAMA; 1997 Oct; 278(15):1237-41. PubMed ID: 9333264
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Multipoint linkage analysis of the pseudoautosomal regions, using affected sibling pairs.
    Dupuis J; Van Eerdewegh P
    Am J Hum Genet; 2000 Aug; 67(2):462-75. PubMed ID: 10869236
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A study comparing precision of the maximum multipoint heterogeneity LOD statistic to three model-free multipoint linkage methods.
    Finch SJ; Chen CH; Gordon D; Mendell NR
    Genet Epidemiol; 2001 Dec; 21(4):315-25. PubMed ID: 11754467
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Allele-sharing models: LOD scores and accurate linkage tests.
    Kong A; Cox NJ
    Am J Hum Genet; 1997 Nov; 61(5):1179-88. PubMed ID: 9345087
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Model-based linkage analyses confirm chromosome 19q13.3 as a susceptibility locus for intracranial aneurysm.
    Mineharu Y; Inoue K; Inoue S; Yamada S; Nozaki K; Hashimoto N; Koizumi A
    Stroke; 2007 Apr; 38(4):1174-8. PubMed ID: 17322081
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Using risk calculation to implement an extended relative pair analysis.
    Curtis D; Sham PC
    Ann Hum Genet; 1994 May; 58(2):151-62. PubMed ID: 7979159
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Affected-sib-pair test for linkage based on constraints for identical-by-descent distributions corresponding to disease models with imprinting.
    Knapp M; Strauch K
    Genet Epidemiol; 2004 May; 26(4):273-85. PubMed ID: 15095387
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mapping of a gene for X-linked agammaglobulinemia and evidence for genetic heterogeneity.
    Mensink EJ; Thompson A; Schot JD; van de Greef WM; Sandkuyl LA; Schuurman RK
    Hum Genet; 1986 Aug; 73(4):327-32. PubMed ID: 3502688
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic linkage studies of X-linked hypophosphataemic rickets in a Saudi Arabian family.
    Thakker RV; Farmery MR; Sakati NA; Milner RD
    Clin Endocrinol (Oxf); 1992 Oct; 37(4):338-43. PubMed ID: 1483289
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Efficiency of typing unaffected relatives in an affected-sib-pair linkage study with single-locus and multiple tightly linked markers.
    Holmans P; Clayton D
    Am J Hum Genet; 1995 Nov; 57(5):1221-32. PubMed ID: 7485174
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Linkage and association with type 1 diabetes on chromosome 1q42.
    Ewens KG; Johnson LN; Wapelhorst B; O'Brien K; Gutin S; Morrison VA; Street C; Gregory SG; Spielman RS; Concannon P
    Diabetes; 2002 Nov; 51(11):3318-25. PubMed ID: 12401725
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.