BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

161 related articles for article (PubMed ID: 2066097)

  • 1. Deletion of chromosome 21 and normal intelligence: molecular definition of the lesion.
    Korenberg JR; Kalousek DK; Anneren G; Pulst SM; Hall JG; Epstein CJ; Cox DR
    Hum Genet; 1991 Jun; 87(2):112-8. PubMed ID: 2066097
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotype.
    Korenberg JR; Kawashima H; Pulst SM; Ikeuchi T; Ogasawara N; Yamamoto K; Schonberg SA; West R; Allen L; Magenis E
    Am J Hum Genet; 1990 Aug; 47(2):236-46. PubMed ID: 2143053
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Down syndrome: toward a molecular definition of the phenotype.
    Korenberg JR; Kawashima H; Pulst SM; Allen L; Magenis E; Epstein CJ
    Am J Med Genet Suppl; 1990; 7():91-7. PubMed ID: 2149983
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The Alzheimer amyloid precursor protein maps to human chromosome 21 bands q21.105-q21.05.
    Korenberg JR; Pulst SM; Neve RL; West R
    Genomics; 1989 Jul; 5(1):124-7. PubMed ID: 2527801
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Stable ring chromosome 21: molecular and clinical definition of the lesion.
    Falik-Borenstein TC; Pribyl TM; Pulst SM; Van Dyke DL; Weiss L; Chu ML; Kraus J; Marshak D; Korenberg JR
    Am J Med Genet; 1992 Jan; 42(1):22-8. PubMed ID: 1308361
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Regional assignment of six polymorphic DNA sequences on chromosome 21 by in situ hybridization to normal and rearranged chromosomes.
    Münke M; Foellmer B; Watkins PC; Cowan JM; Carroll AJ; Gusella JF; Francke U
    Am J Hum Genet; 1988 Apr; 42(4):542-9. PubMed ID: 3348217
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Physical findings in 21q22 deletion suggest critical region for 21q- phenotype in q22.
    Theodoropoulos DS; Cowan JM; Elias ER; Cole C
    Am J Med Genet; 1995 Nov; 59(2):161-3. PubMed ID: 8588579
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A fine-structure deletion map of human chromosome 11p: analysis of J1 series hybrids.
    Glaser T; Housman D; Lewis WH; Gerhard D; Jones C
    Somat Cell Mol Genet; 1989 Nov; 15(6):477-501. PubMed ID: 2595451
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Application of molecular and somatic cell genetics to the study of chromosome 21.
    Law ML; Van Keuren M
    Ann N Y Acad Sci; 1986; 477():151-9. PubMed ID: 2880544
    [TBL] [Abstract][Full Text] [Related]  

  • 10. No significant effect of monosomy for distal 21q22.3 on the Down syndrome phenotype in "mirror" duplications of chromosome 21.
    Pangalos C; Théophile D; Sinet PM; Marks A; Stamboulieh-Abazis D; Chettouh Z; Prieur M; Verellen C; Rethoré MO; Lejeune J
    Am J Hum Genet; 1992 Dec; 51(6):1240-50. PubMed ID: 1463008
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Panel of aneuploid cell lines for physical mapping of the proximal long arm of human chromosome 21.
    Pulst SM; Korenberg JR
    Am J Med Genet Suppl; 1990; 7():137-40. PubMed ID: 2127362
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification and molecular cytogenetic characterization of a novel complex Y chromosome rearrangement in a boy with disorder of sexual development.
    Dutta UR; Pidugu VK; Goud ChV; Hoefers C; Hagemann M; Dalal A
    Gene; 2013 May; 519(2):374-80. PubMed ID: 23428792
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Characterization of an unusual and complex chromosome 21 rearrangement using somatic cell genetics and cloned DNA probes.
    Van Keuren ML; Stewart GD; Bradley CM; Kurnit DM; Neve RL; Watkins PC; Tanzi RE; Gusella JF; Patterson D
    Am J Med Genet; 1989 Jul; 33(3):369-75. PubMed ID: 2529766
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Normal superoxide dismutase-1 (SOD-1) activity with deletion of chromosome band 21q21 supports localization of SOD-1 locus to 21q22.
    Wulfsberg EA; Carrel RE; Klisak IJ; O'Brien TJ; Sykes JA; Sparkes RS
    Hum Genet; 1983; 64(3):271-2. PubMed ID: 6885070
    [TBL] [Abstract][Full Text] [Related]  

  • 15. De novo 9-break-event in one chromosome 21 combined with a microdeletion in 21q22.11 in a mentally retarded boy with short stature.
    Weise A; Rittinger O; Starke H; Ziegler M; Claussen U; Liehr T
    Cytogenet Genome Res; 2003; 103(1-2):14-6. PubMed ID: 15004457
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Down syndrome--a gene dosage disease caused by trisomy of genes within a small segment of the long arm of chromosome 21, exemplified by the study of effects from the superoxide-dismutase type 1 (SOD-1) gene.
    Annerén G; Edman B
    APMIS Suppl; 1993; 40():71-9. PubMed ID: 8311993
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Tetrasomy 21 pter-->q22.1 and Down syndrome: molecular definition of the region.
    Daumer-Haas C; Schuffenhauer S; Walther JU; Schipper RD; Porstmann T; Korenberg JR
    Am J Med Genet; 1994 Dec; 53(4):359-65. PubMed ID: 7532356
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Down syndrome with duplication of a region of chromosome 21 containing the CuZn superoxide dismutase gene without detectable karyotypic abnormality.
    Huret JL; Delabar JM; Marlhens F; Aurias A; Nicole A; Berthier M; Tanzer J; Sinet PM
    Hum Genet; 1987 Mar; 75(3):251-7. PubMed ID: 2951317
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical, cytogenetic, and molecular evaluation of a patient with partial trisomy 21 (21q11-q22) lacking the classical Down syndrome phenotype.
    Williams CA; Frias JL; McCormick MK; Antonarakis SE; Cantu ES
    Am J Med Genet Suppl; 1990; 7():110-4. PubMed ID: 2149936
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Sequence-based, in situ detection of chromosomal abnormalities at high resolution.
    Knoll JH; Rogan PK
    Am J Med Genet A; 2003 Sep; 121A(3):245-57. PubMed ID: 12923866
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.