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 *

124 related articles for article (PubMed ID: 10848501)

  • 1. Interpretation of linkage data for a Huntington-like disorder mapping to 4p15.3.
    Lesperance MM; Burmeister M
    Am J Hum Genet; 2000 Jul; 67(1):262-3. PubMed ID: 10848501
    [No Abstract]   [Full Text] [Related]  

  • 2. Localization of the gene for a novel autosomal recessive neurodegenerative Huntington-like disorder to 4p15.3.
    Kambouris M; Bohlega S; Al-Tahan A; Meyer BF
    Am J Hum Genet; 2000 Feb; 66(2):445-52. PubMed ID: 10677304
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Neurodegenerative Huntington-like disorder.
    Bohlega S; Al-Tahan A; Kambouris M; Divakaran M
    Mov Disord; 2001 May; 16(3):533-4. PubMed ID: 11391753
    [No Abstract]   [Full Text] [Related]  

  • 4. Detection of disease genes by use of family data. I. Likelihood-based theory.
    Whittemore AS; Tu IP
    Am J Hum Genet; 2000 Apr; 66(4):1328-40. PubMed ID: 10739758
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genome scan for predisposing loci for distal interphalangeal joint osteoarthritis: evidence for a locus on 2q.
    Leppävuori J; Kujala U; Kinnunen J; Kaprio J; Nissilä M; Heliövaara M; Klinger N; Partanen J; Terwilliger JD; Peltonen L
    Am J Hum Genet; 1999 Oct; 65(4):1060-7. PubMed ID: 10486325
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A Huntington disease-like neurodegenerative disorder maps to chromosome 20p.
    Xiang F; Almqvist EW; Huq M; Lundin A; Hayden MR; Edström L; Anvret M; Zhang Z
    Am J Hum Genet; 1998 Nov; 63(5):1431-8. PubMed ID: 9792871
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic linkage of Bietti crystallin corneoretinal dystrophy to chromosome 4q35.
    Jiao X; Munier FL; Iwata F; Hayakawa M; Kanai A; Lee J; Schorderet DF; Chen MS; Kaiser-Kupfer M; Hejtmancik JF
    Am J Hum Genet; 2000 Nov; 67(5):1309-13. PubMed ID: 11001583
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic linkage of the dentinogenesis imperfecta type III locus to chromosome 4q.
    MacDougall M; Jeffords LG; Gu TT; Knight CB; Frei G; Reus BE; Otterud B; Leppert M; Leach RJ
    J Dent Res; 1999 Jun; 78(6):1277-82. PubMed ID: 10371253
    [TBL] [Abstract][Full Text] [Related]  

  • 9. QTL fine mapping by measuring and testing for Hardy-Weinberg and linkage disequilibrium at a series of linked marker loci in extreme samples of populations.
    Deng HW; Chen WM; Recker RR
    Am J Hum Genet; 2000 Mar; 66(3):1027-45. PubMed ID: 10712216
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. DFNA49, a novel locus for autosomal dominant non-syndromic hearing loss, maps proximal to DFNA7/DFNM1 region on chromosome 1q21-q23.
    Moreno-Pelayo MA; Modamio-Høybjør S; Mencía A; del Castillo I; Chardenoux S; Fernández-Burriel M; Lathrop M; Petit C; Moreno F
    J Med Genet; 2003 Nov; 40(11):832-6. PubMed ID: 14627674
    [No Abstract]   [Full Text] [Related]  

  • 12. Detection of tandem duplications and implications for linkage analysis.
    Matise TC; Chakravarti A; Patel PI; Lupski JR; Nelis E; Timmerman V; Van Broeckhoven C; Weeks DE
    Am J Hum Genet; 1994 Jun; 54(6):1110-21. PubMed ID: 8198134
    [TBL] [Abstract][Full Text] [Related]  

  • 13. An examination of linkage of schizophrenia and schizoaffective disorder to the pseudoautosomal region (Xp22.3).
    Crow TJ; Delisi LE; Lofthouse R; Poulter M; Lehner T; Bass N; Shah T; Walsh C; Boccio-Smith A; Shields G
    Br J Psychiatry; 1994 Feb; 164(2):159-64. PubMed ID: 7818635
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Transmission/disequilibrium tests for extended marker haplotypes.
    Clayton D; Jones H
    Am J Hum Genet; 1999 Oct; 65(4):1161-9. PubMed ID: 10486335
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hunting for Huntington's disease.
    Gusella JF; MacDonald ME
    Mol Genet Med; 1993; 3():139-58. PubMed ID: 8220162
    [No Abstract]   [Full Text] [Related]  

  • 16. Comparison of tests for association and linkage in incomplete families.
    Cervino AC; Hill AV
    Am J Hum Genet; 2000 Jul; 67(1):120-32. PubMed ID: 10841813
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic linkage of hyper-IgE syndrome to chromosome 4.
    Grimbacher B; Schäffer AA; Holland SM; Davis J; Gallin JI; Malech HL; Atkinson TP; Belohradsky BH; Buckley RH; Cossu F; Español T; Garty BZ; Matamoros N; Myers LA; Nelson RP; Ochs HD; Renner ED; Wellinghausen N; Puck JM
    Am J Hum Genet; 1999 Sep; 65(3):735-44. PubMed ID: 10441580
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA50, maps to chromosome 7q32 between the DFNB17 and DFNB13 deafness loci.
    Modamio-Høybjør S; Moreno-Pelayo MA; Mencía A; del Castillo I; Chardenoux S; Morais D; Lathrop M; Petit C; Moreno F
    J Med Genet; 2004 Feb; 41(2):e14. PubMed ID: 14757864
    [No Abstract]   [Full Text] [Related]  

  • 19. Optimal ascertainment strategies to detect linkage to common disease alleles.
    Baron M
    Am J Hum Genet; 1999 Apr; 64(4):1243-8. PubMed ID: 10090916
    [No Abstract]   [Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.