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 *

55 related articles for article (PubMed ID: 10088039)

  • 1. Optimization of genome search strategies for homozygosity mapping: influence of marker spacing on power and threshold criteria for identification of candidate regions.
    Génin E; Todorov AA; Clerget-Darpoux F
    Ann Hum Genet; 1998 Sep; 62(Pt 5):419-29. PubMed ID: 10088039
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Application of homozygosity mapping to the fine mapping of the osteoporosis-pseudoglioma syndrome locus].
    Gong YQ; Li JX; Liu QJ; Chen BX; Guo CH; Gao GM
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Feb; 20(1):53-5. PubMed ID: 12579502
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Homozygosity mapping in a family presenting with schizophrenia, epilepsy and hearing impairment.
    Knight HM; Maclean A; Irfan M; Naeem F; Cass S; Pickard BS; Muir WJ; Blackwood DH; Ayub M
    Eur J Hum Genet; 2008 Jun; 16(6):750-8. PubMed ID: 18322454
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Homozygosity mapping of familial glioma in Northern Sweden.
    Malmer B; Haraldsson S; Einarsdottir E; Lindgren P; Holmberg D
    Acta Oncol; 2005; 44(2):114-9. PubMed ID: 15788289
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Computing probabilities of homozygosity by descent.
    Schäffer AA
    Genet Epidemiol; 1999; 16(2):135-49. PubMed ID: 10030397
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prospects for association-based fine mapping of a susceptibility gene for a complex disease.
    Kaplan N; Morris R
    Theor Popul Biol; 2001 Nov; 60(3):181-91. PubMed ID: 11855952
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Studies of marker screening efficiency and corresponding influencing factors in QTL composite interval mapping].
    Gao YM; Wan P
    Yi Chuan Xue Bao; 2002 Jun; 29(6):555-61. PubMed ID: 12096636
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Issues concerning association studies for fine mapping a susceptibility gene for a complex disease.
    Kaplan N; Morris R
    Genet Epidemiol; 2001 May; 20(4):432-57. PubMed ID: 11319784
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Consanguinity and the transmission/disequilibrium test for allelic association.
    Bennett S; Curnow RN
    Genet Epidemiol; 2001 Jul; 21(1):68-77. PubMed ID: 11443735
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Localisation of a gene for mucopolysaccharidosis IIIC to the pericentromeric region of chromosome 8.
    Ausseil J; Loredo-Osti JC; Verner A; Darmond-Zwaig C; Maire I; Poorthuis B; van Diggelen OP; Hudson TJ; Fujiwara TM; Morgan K; Pshezhetsky AV
    J Med Genet; 2004 Dec; 41(12):941-5. PubMed ID: 15591281
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Localization of the gene for autosomal recessive congenital hereditary endothelial dystrophy (CHED2) to chromosome 20 by homozygosity mapping.
    Hand CK; Harmon DL; Kennedy SM; FitzSimon JS; Collum LM; Parfrey NA
    Genomics; 1999 Oct; 61(1):1-4. PubMed ID: 10512674
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Novel congenital myopathy locus identified in Native American Indians at 12q13.13-14.1.
    Stamm DS; Powell CM; Stajich JM; Zismann VL; Stephan DA; Chesnut B; Aylsworth AS; Kahler SG; Deak KL; Gilbert JR; Speer MC
    Neurology; 2008 Nov; 71(22):1764-9. PubMed ID: 18843099
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A gene causing autosomal recessive cataract maps to the short arm of chromosome 3.
    Pras E; Pras E; Bakhan T; Levy-Nissenbaum E; Lahat H; Assia EI; Garzozi HJ; Kastner DL; Goldman B; Frydman M
    Isr Med Assoc J; 2001 Aug; 3(8):559-62. PubMed ID: 11519376
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of a chromosome 8p locus for early-onset coronary heart disease in a French Canadian population.
    Engert JC; Lemire M; Faith J; Brisson D; Fujiwara TM; Roslin NM; Brewer CG; Montpetit A; Darmond-Zwaig C; Renaud Y; Doré C; Bailey SD; Verner A; Tremblay G; St-Pierre J; Bétard C; Platko J; Rioux JD; Morgan K; Hudson TJ; Gaudet D
    Eur J Hum Genet; 2008 Jan; 16(1):105-14. PubMed ID: 17805225
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Global tests for linkage.
    el Galta R; van Houwelingen HC; Houwing-Duistermaat JJ
    Biom J; 2009 Feb; 51(1):70-83. PubMed ID: 19197957
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Lod scores for gene mapping in the presence of marker map uncertainty.
    Stringham HM; Boehnke M
    Genet Epidemiol; 2001 Jul; 21(1):31-9. PubMed ID: 11443732
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. A nearest-neighboring-end algorithm for genetic mapping.
    Crane CF; Crane YM
    Bioinformatics; 2005 Apr; 21(8):1579-91. PubMed ID: 15564296
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identity-by-descent approach to gene localisation in eight individuals affected by keratoconus from north-west Tasmania, Australia.
    Fullerton J; Paprocki P; Foote S; Mackey DA; Williamson R; Forrest S
    Hum Genet; 2002 May; 110(5):462-70. PubMed ID: 12073017
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A genome-wide scan maps a novel high myopia locus to 5p15.
    Lam CY; Tam PO; Fan DS; Fan BJ; Wang DY; Lee CW; Pang CP; Lam DS
    Invest Ophthalmol Vis Sci; 2008 Sep; 49(9):3768-78. PubMed ID: 18421076
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 3.