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 *

81 related articles for article (PubMed ID: 8556826)

  • 21. Localization of a gene for Waardenburg syndrome type I.
    Read AP; Foy C; Newton V; Harris R
    Ann N Y Acad Sci; 1991; 630():143-51. PubMed ID: 1952585
    [No Abstract]   [Full Text] [Related]  

  • 22. Confirmation of the location of a Waardenburg syndrome type I mutation on human chromosome 2q. Tight linkage to FN1 and ALPP.
    Asher JH; Morell R; Friedman TB
    Ann N Y Acad Sci; 1991; 630():295-7. PubMed ID: 1683205
    [No Abstract]   [Full Text] [Related]  

  • 23. DNA polymorphism and linkage disequilibrium within the apolipoprotein CII locus on human chromosome 19.
    MacKenzie AE; MacLeod HL; Leblond SC; Monteith N; Lahey D; Korneluk RG
    Hum Hered; 1991; 41(3):188-94. PubMed ID: 1682238
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A Bam H1 RFLP in the human alpha 2 (X1) (COL 11A2) gene.
    Priestley LM; Sykes BC; Cheah KS
    Nucleic Acids Res; 1990 Feb; 18(3):689. PubMed ID: 1968625
    [No Abstract]   [Full Text] [Related]  

  • 25. A polymorphic DNA marker on chromosome 10 linked to RBP3 on the MEN2A side.
    Wu J; Cavenee WK; Miki T; Kidd KK
    Cytogenet Cell Genet; 1988; 48(4):246-7. PubMed ID: 2907872
    [No Abstract]   [Full Text] [Related]  

  • 26. Assignment of the human gene for receptor-type protein tyrosine phosphatase IA-2 (PTPRN) to chromosome region 2q35 --> q36.1 and identification of an intragenic genetic marker.
    van den Maagdenberg AM; Olde Weghuis D; Rijss J; van de Wetering RA; Wieringa B; Geurts van Kessel A; Hendriks WJ
    Cytogenet Cell Genet; 1996; 73(1-2):145-8. PubMed ID: 8646884
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Identification of a new mutation in the alpha4(IV) collagen gene in a family with autosomal dominant Alport syndrome and hypercholesterolaemia.
    Ciccarese M; Casu D; Ki Wong F; Faedda R; Arvidsson S; Tonolo G; Luthman H; Satta A
    Nephrol Dial Transplant; 2001 Oct; 16(10):2008-12. PubMed ID: 11572889
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Polymorphism of DNA sequence in the human pro alpha 2(I) collagen gene.
    Grobler-Rabie AF; Brebner DK; Vandenplas S; Wallis G; Dalgleish R; Kaufman RE; Bester AJ; Mathew CG; Boyd CD
    J Med Genet; 1985 Jun; 22(3):182-6. PubMed ID: 2409282
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Regional mapping of loci from human chromosome 2q to sheep chromosome 2q.
    Ansari HA; Pearce PD; Maher DW; Malcolm AA; Wood NJ; Phua SH; Broad TE
    Genomics; 1994 Mar; 20(1):122-4. PubMed ID: 8020939
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A highly polymorphic locus on chromosome 11 which has homology to a collagen triple-helix coding sequence.
    Brookes AJ; Hedge PH; Solomon E
    Nucleic Acids Res; 1989 Feb; 17(4):1792. PubMed ID: 2564196
    [No Abstract]   [Full Text] [Related]  

  • 31. Report and abstracts of the Second International Workshop on Human Chromosome 2 Mapping.
    Spurr NK; Cox S; Naylor S
    Cytogenet Cell Genet; 1993; 64(2):69-92. PubMed ID: 8334898
    [No Abstract]   [Full Text] [Related]  

  • 32. No evidence of association of chromosome 2q with Type I diabetes in the Basque population.
    Pérez de Nanclares G; Bilbao JR; Nisticò L; Buzzetti R; Larsen ZM; Pociot F; Castaño L
    Diabetologia; 1999 Jan; 42(1):119-20. PubMed ID: 10027592
    [No Abstract]   [Full Text] [Related]  

  • 33. Oguchi disease: suggestion of linkage to markers on chromosome 2q.
    Maw MA; John S; Jablonka S; Müller B; Kumaramanickavel G; Oehlmann R; Denton MJ; Gal A
    J Med Genet; 1995 May; 32(5):396-8. PubMed ID: 7616550
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A novel BamHI polymorphism for the human transforming growth factor alpha gene (TGF-alpha).
    Qian JF; May E; Feingold J; Stoll C
    Nucleic Acids Res; 1991 Dec; 19(23):6665. PubMed ID: 1684429
    [No Abstract]   [Full Text] [Related]  

  • 35. DNA-polymorphism of type I collagen gene detected with Bgl II in the genetically isolated Finnish population.
    Ahti H; Palotie A; Peltonen L; Ramirez F
    Hum Genet; 1987 Jan; 75(1):79-80. PubMed ID: 3026951
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Physical and genetic mapping of the dipeptidase gene DPEP1 to 16q24.3.
    Austruy E; Jeanpierre C; Antignac C; Whitmore SA; Van Cong N; Bernheim A; Callen DF; Junien C
    Genomics; 1993 Mar; 15(3):684-7. PubMed ID: 7682195
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Physical and linkage mapping of the gene for the alpha3 chain of type IX collagen, COL9A3, to human chromosome 20q13.3.
    Tiller GE; Warman ML; Gong Y; Knoll JH; Mayne R; Brewton RG
    Cytogenet Cell Genet; 1998; 81(3-4):205-7. PubMed ID: 9730604
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Myelomeningocele and Waardenburg syndrome (type 3) in patients with interstitial deletions of 2q35 and the PAX3 gene: possible digenic inheritance of a neural tube defect.
    Nye JS; Balkin N; Lucas H; Knepper PA; McLone DG; Charrow J
    Am J Med Genet; 1998 Feb; 75(4):401-8. PubMed ID: 9482647
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Identification of a polymorphic CA repeat in the COL6A2 gene on human chromosome 21q22.3.
    Comeglio P; Saitta B; Pepe G; Chu ML
    Hum Hered; 1996; 46(4):239-40. PubMed ID: 8807328
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Homozygosity mapping of achromatopsia to chromosome 2 using DNA pooling.
    Arbour NC; Zlotogora J; Knowlton RG; Merin S; Rosenmann A; Kanis AB; Rokhlina T; Stone EM; Sheffield VC
    Hum Mol Genet; 1997 May; 6(5):689-94. PubMed ID: 9158143
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.