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 *

99 related articles for article (PubMed ID: 7874123)

  • 1. Linkage of a locus for carbohydrate-deficient glycoprotein syndrome type I (CDG1) to chromosome 16p, and linkage disequilibrium to microsatellite marker D16S406.
    Martinsson T; Bjursell C; Stibler H; Kristiansson B; Skovby F; Jaeken J; Blennow G; Strömme P; Hanefeld F; Wahlström J
    Hum Mol Genet; 1994 Nov; 3(11):2037-42. PubMed ID: 7874123
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Fine mapping of the gene for carbohydrate-deficient glycoprotein syndrome, type I (CDG1): linkage disequilibrium and founder effect in Scandinavian families.
    Bjursell C; Stibler H; Wahlström J; Kristiansson B; Skovby F; Strömme P; Blennow G; Martinsson T
    Genomics; 1997 Feb; 39(3):247-53. PubMed ID: 9119361
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Evidence for genetic heterogeneity in the carbohydrate-deficient glycoprotein syndrome type I (CDG1).
    Matthijs G; Legius E; Schollen E; Vandenberk P; Jaeken J; Barone R; Fiumara A; Visser G; Lambert M; Cassiman JJ
    Genomics; 1996 Aug; 35(3):597-9. PubMed ID: 8812498
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Linkage disequilibrium in inbred North African families allows fine genetic and physical mapping of triple A syndrome.
    Hadj-Rabia S; Salomon R; Pelet A; Penet C; Rotschild A; de Laët MH; Chaouachi B; Hannachi R; Bakiri F; Brauner R; Chaussain JL; Munnich A; Lyonnet S
    Eur J Hum Genet; 2000 Aug; 8(8):613-20. PubMed ID: 10951524
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Localization of a gene for familial juvenile hyperuricemic nephropathy causing underexcretion-type gout to 16p12 by genome-wide linkage analysis of a large family.
    Kamatani N; Moritani M; Yamanaka H; Takeuchi F; Hosoya T; Itakura M
    Arthritis Rheum; 2000 Apr; 43(4):925-9. PubMed ID: 10765940
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Detailed mapping of the phosphomannomutase 2 (PMM2) gene and mutation detection enable improved analysis for Scandinavian CDG type I families.
    Bjursell C; Wahlström J; Berg K; Stibler H; Kristiansson B; Matthijs G; Martinsson T
    Eur J Hum Genet; 1998; 6(6):603-11. PubMed ID: 9887379
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Linkage mapping of new X-linked juvenile retinoschisis kindreds using microsatellite markers.
    Shastry BS; Hejtmancik FJ; Margherio RT; Trese MT
    Biochem Biophys Res Commun; 1996 Mar; 220(3):824-7. PubMed ID: 8607849
    [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. An efficient, robust and unified method for mapping complex traits (III): combined linkage/linkage-disequilibrium analysis.
    Zhao LP; Quiaoit F; Aragaki C; Hsu L
    Am J Med Genet; 1999 Jun; 84(5):433-53. PubMed ID: 10360398
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Refinement of the gene locus for autosomal recessive juvenile parkinsonism (AR-JP) on chromosome 6q25.2-27 and identification of markers exhibiting linkage disequilibrium.
    Saito M; Matsumine H; Tanaka H; Ishikawa A; Shimoda-Matsubayashi S; Schäffer AA; Mizuno Y; Tsuji S
    J Hum Genet; 1998; 43(1):22-31. PubMed ID: 9609994
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Refined genetic mapping of autosomal recessive chronic distal spinal muscular atrophy to chromosome 11q13.3 and evidence of linkage disequilibrium in European families.
    Viollet L; Zarhrate M; Maystadt I; Estournet-Mathiaut B; Barois A; Desguerre I; Mayer M; Chabrol B; LeHeup B; Cusin V; Billette De Villemeur T; Bonneau D; Saugier-Veber P; Touzery-De Villepin A; Delaubier A; Kaplan J; Jeanpierre M; Feingold J; Munnich A
    Eur J Hum Genet; 2004 Jun; 12(6):483-8. PubMed ID: 15054395
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The gene for Machado-Joseph disease maps to human chromosome 14q.
    Takiyama Y; Nishizawa M; Tanaka H; Kawashima S; Sakamoto H; Karube Y; Shimazaki H; Soutome M; Endo K; Ohta S
    Nat Genet; 1993 Jul; 4(3):300-4. PubMed ID: 8358439
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutations in PMM2, a phosphomannomutase gene on chromosome 16p13, in carbohydrate-deficient glycoprotein type I syndrome (Jaeken syndrome).
    Matthijs G; Schollen E; Pardon E; Veiga-Da-Cunha M; Jaeken J; Cassiman JJ; Van Schaftingen E
    Nat Genet; 1997 May; 16(1):88-92. PubMed ID: 9140401
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic linkage analysis of familial amyotrophic lateral sclerosis using human chromosome 21 microsatellite DNA markers.
    Rosen DR; Sapp P; O'Regan J; McKenna-Yasek D; Schlumpf KS; Haines JL; Gusella JF; Horvitz HR; Brown RH
    Am J Med Genet; 1994 May; 51(1):61-9. PubMed ID: 7913294
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Absence of homozygosity for predominant mutations in PMM2 in Danish patients with carbohydrate-deficient glycoprotein syndrome type 1.
    Kjaergaard S; Skovby F; Schwartz M
    Eur J Hum Genet; 1998; 6(4):331-6. PubMed ID: 9781039
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q.
    Guilford P; Ben Arab S; Blanchard S; Levilliers J; Weissenbach J; Belkahia A; Petit C
    Nat Genet; 1994 Jan; 6(1):24-8. PubMed ID: 8136828
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Refined localization of the Batten disease gene (CLN3) by haplotype and linkage disequilibrium mapping to D16S288-D16S383 and exclusion from this region of a variant form of Batten disease with granular osmiophilic deposits.
    Mitchison HM; O'Rawe AM; Lerner TJ; Taschner PE; Schlumpf K; D'Arigo K; de Vos N; Gormally E; Phillips HA; Thompson AD
    Am J Med Genet; 1995 Jun; 57(2):312-5. PubMed ID: 7668353
    [TBL] [Abstract][Full Text] [Related]  

  • 18. First genomic localization of oculo-oto-dental syndrome with linkage to chromosome 20q13.1.
    Vieira H; Gregory-Evans K; Lim N; Brookes JL; Brueton LA; Gregory-Evans CY
    Invest Ophthalmol Vis Sci; 2002 Aug; 43(8):2540-5. PubMed ID: 12147582
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Human rod monochromacy: linkage analysis and mapping of a cone photoreceptor expressed candidate gene on chromosome 2q11.
    Wissinger B; Jägle H; Kohl S; Broghammer M; Baumann B; Hanna DB; Hedels C; Apfelstedt-Sylla E; Randazzo G; Jacobson SG; Zrenner E; Sharpe LT
    Genomics; 1998 Aug; 51(3):325-31. PubMed ID: 9721202
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31-33.
    Toda T; Segawa M; Nomura Y; Nonaka I; Masuda K; Ishihara T; Sakai M; Tomita I; Origuchi Y; Suzuki M [corrected to Sakai M]
    Nat Genet; 1993 Nov; 5(3):283-6. PubMed ID: 8275093
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.