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 *

179 related articles for article (PubMed ID: 7887419)

  • 1. Batten disease gene, CLN3: linkage disequilibrium mapping in the Finnish population, and analysis of European haplotypes.
    Mitchison HM; O'Rawe AM; Taschner PE; Sandkuijl LA; Santavuori P; de Vos N; Breuning MH; Mole SE; Gardiner RM; Järvelä IE
    Am J Hum Genet; 1995 Mar; 56(3):654-62. PubMed ID: 7887419
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Genetic mapping of the Batten disease locus (CLN3) to the interval D16S288-D16S383 by analysis of haplotypes and allelic association.
    Mitchison HM; Taschner PE; O'Rawe AM; de Vos N; Phillips HA; Thompson AD; Kozman HM; Haines JL; Schlumpf K; D'Arigo K
    Genomics; 1994 Jul; 22(2):465-8. PubMed ID: 7806237
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Fine genetic mapping of the Batten disease locus (CLN3) by haplotype analysis and demonstration of allelic association with chromosome 16p microsatellite loci.
    Mitchison HM; Thompson AD; Mulley JC; Kozman HM; Richards RI; Callen DF; Stallings RL; Doggett NA; Attwood J; McKay TR
    Genomics; 1993 May; 16(2):455-60. PubMed ID: 8314582
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Linkage disequilibrium between the juvenile neuronal ceroid lipofuscinosis gene and marker loci on chromosome 16p 12.1.
    Lerner TJ; Boustany RM; MacCormack K; Gleitsman J; Schlumpf K; Breakefield XO; Gusella JF; Haines JL
    Am J Hum Genet; 1994 Jan; 54(1):88-94. PubMed ID: 8279474
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Carrier detection of Batten disease (juvenile neuronal ceroid-lipofuscinosis).
    Taschner PE; de Vos N; Post JG; Meijers-Heijboer EJ; Hofman I; Loonen MC; Pinckers AJ; Bleeker-Wagemakers EM; Gardiner RM; Breuning MH
    Am J Med Genet; 1995 Jun; 57(2):333-7. PubMed ID: 7668358
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Chromosome 16 microdeletion in a patient with juvenile neuronal ceroid lipofuscinosis (Batten disease).
    Taschner PE; de Vos N; Thompson AD; Callen DF; Doggett N; Mole SE; Dooley TP; Barth PG; Breuning MH
    Am J Hum Genet; 1995 Mar; 56(3):663-8. PubMed ID: 7887420
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Physical map of the region containing the gene for Batten disease (CLN3).
    Järvelä IE; Mitchison HM; Callen DF; Lerner TJ; Doggett NA; Taschner PE; Gardiner RM; Mole SE
    Am J Med Genet; 1995 Jun; 57(2):316-9. PubMed ID: 7668354
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The age of human mutation: genealogical and linkage disequilibrium analysis of the CLN5 mutation in the Finnish population.
    Varilo T; Savukoski M; Norio R; Santavuori P; Peltonen L; Järvelä I
    Am J Hum Genet; 1996 Mar; 58(3):506-12. PubMed ID: 8644710
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Infantile neuronal ceroid-lipofuscinosis is not an allelic form of Batten disease: exclusion of chromosome 16 region with linkage analyses.
    Jokiaho I; Puhakka L; Santavuori P; Manninen T; Nyman K; Peltonen L
    Genomics; 1990 Oct; 8(2):391-3. PubMed ID: 2249855
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Batten disease (Spielmeyer-Vogt disease, juvenile onset neuronal ceroid-lipofuscinosis) gene (CLN3) maps to human chromosome 16.
    Gardiner M; Sandford A; Deadman M; Poulton J; Cookson W; Reeders S; Jokiaho I; Peltonen L; Eiberg H; Julier C
    Genomics; 1990 Oct; 8(2):387-90. PubMed ID: 2249854
    [TBL] [Abstract][Full Text] [Related]  

  • 12. YAC and cosmid contigs spanning the Batten disease (CLN3) region at 16p12.1-p11.2.
    Järvelä IE; Mitchison HM; O'Rawe AM; Munroe PB; Taschner PE; de Vos N; Lerner TJ; D'Arigo KL; Callen DF; Thompson AD
    Genomics; 1995 Sep; 29(2):478-89. PubMed ID: 8666398
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Isolation of a novel gene underlying Batten disease, CLN3. The International Batten Disease Consortium.
    Cell; 1995 Sep; 82(6):949-57. PubMed ID: 7553855
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Infantile neuronal ceroid lipofuscinosis (CLN1): linkage disequilibrium in the Finnish population and evidence that variant late infantile form (variant CLN2) represents a nonallelic locus.
    Järvelä I
    Genomics; 1991 Jun; 10(2):333-7. PubMed ID: 2071142
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A variant form of late infantile neuronal ceroid lipofuscinosis (CLN5) is not an allelic form of Batten (Spielmeyer-Vogt-Sjögren, CLN3) disease: exclusion of linkage to the CLN3 region of chromosome 16.
    Williams R; Santavuori P; Peltonen L; Gardiner RM; Järvelä I
    Genomics; 1994 Mar; 20(2):289-90. PubMed ID: 8020979
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mapping the gene for juvenile onset neuronal ceroid lipofuscinosis to chromosome 16 by linkage analysis.
    Gardiner RM
    Am J Med Genet; 1992 Feb; 42(4):539-41. PubMed ID: 1351702
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Profound infantile neuroretinal dysfunction in a heterozygote for the CLN3 genetic defect.
    de los Reyes E; Dyken PR; Phillips P; Brodsky M; Bates S; Glasier C; Mrak RE
    J Child Neurol; 2004 Jan; 19(1):42-6. PubMed ID: 15032383
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Rapid diagnostic test for the major mutation underlying Batten disease.
    Järvelä I; Mitchison HM; Munroe PB; O'Rawe AM; Mole SE; Syvänen AC
    J Med Genet; 1996 Dec; 33(12):1041-2. PubMed ID: 9004140
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Regional mapping of the Batten disease locus (CLN3) to human chromosome 16p12.
    Callen DF; Baker E; Lane S; Nancarrow J; Thompson A; Whitmore SA; MacLennan DH; Berger R; Cherif D; Järvelä I
    Am J Hum Genet; 1991 Dec; 49(6):1372-7. PubMed ID: 1746562
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutated genes in juvenile and variant late infantile neuronal ceroid lipofuscinoses encode lysosomal proteins.
    Vesa J; Peltonen L
    Curr Mol Med; 2002 Aug; 2(5):439-44. PubMed ID: 12125809
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.