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 *

286 related articles for article (PubMed ID: 11584295)

  • 1. Segmental duplications: an 'expanding' role in genomic instability and disease.
    Emanuel BS; Shaikh TH
    Nat Rev Genet; 2001 Oct; 2(10):791-800. PubMed ID: 11584295
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular mechanisms for CMT1A duplication and HNPP deletion.
    Boerkoel CF; Inoue K; Reiter LT; Warner LE; Lupski JR
    Ann N Y Acad Sci; 1999 Sep; 883():22-35. PubMed ID: 10586226
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Characterisation of interstitial duplications and triplications of chromosome 15q11-q13.
    Roberts SE; Dennis NR; Browne CE; Willatt L; Woods G; Cross I; Jacobs PA; Thomas S
    Hum Genet; 2002 Mar; 110(3):227-34. PubMed ID: 11935334
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genomics. DNA duplications and deletions help determine health.
    Cohen J
    Science; 2007 Sep; 317(5843):1315-7. PubMed ID: 17823326
    [No Abstract]   [Full Text] [Related]  

  • 5. Parental and chromosomal origins of microdeletion and duplication syndromes involving 7q11.23, 15q11-q13 and 22q11.
    Thomas NS; Durkie M; Potts G; Sandford R; Van Zyl B; Youings S; Dennis NR; Jacobs PA
    Eur J Hum Genet; 2006 Jul; 14(7):831-7. PubMed ID: 16617304
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Chromosomal abnormalities and genomic disorders].
    Inoue K
    Nihon Rinsho; 2005 Dec; 63 Suppl 12():64-9. PubMed ID: 16416772
    [No Abstract]   [Full Text] [Related]  

  • 7. Microdeletion and microduplication syndromes.
    Malcolm S
    Prenat Diagn; 1996 Dec; 16(13):1213-9. PubMed ID: 9061752
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders.
    Depienne C; Moreno-De-Luca D; Heron D; Bouteiller D; Gennetier A; Delorme R; Chaste P; Siffroi JP; Chantot-Bastaraud S; Benyahia B; Trouillard O; Nygren G; Kopp S; Johansson M; Rastam M; Burglen L; Leguern E; Verloes A; Leboyer M; Brice A; Gillberg C; Betancur C
    Biol Psychiatry; 2009 Aug; 66(4):349-59. PubMed ID: 19278672
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Molecular advances in "non-mendelian" genetics. Implications for pediatrics].
    Pérez Jurado LA
    An Esp Pediatr; 1993 Jun; 38(6):479-87. PubMed ID: 8368674
    [No Abstract]   [Full Text] [Related]  

  • 10. Analysis of 17p11.2 chromosome region rearrangements in CMT1 patients from Ukraine.
    Hryshchenko NV; Livshits LA
    Tsitol Genet; 2009; 43(1):36-41. PubMed ID: 19663313
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Segment duplications in the human genome].
    Lakrua ME; Oparina NIu; Mashkova TD
    Mol Biol (Mosk); 2003; 37(2):212-20. PubMed ID: 12723468
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Role of genomic architecture in PLP1 duplication causing Pelizaeus-Merzbacher disease.
    Lee JA; Inoue K; Cheung SW; Shaw CA; Stankiewicz P; Lupski JR
    Hum Mol Genet; 2006 Jul; 15(14):2250-65. PubMed ID: 16774974
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [New developments in cytogenetics].
    Turleau C; Vekemans M
    Med Sci (Paris); 2005 Nov; 21(11):940-6. PubMed ID: 16274645
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of human haploinsufficient genes and their genomic proximity to segmental duplications.
    Dang VT; Kassahn KS; Marcos AE; Ragan MA
    Eur J Hum Genet; 2008 Nov; 16(11):1350-7. PubMed ID: 18523451
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Visualization of the CMT1A duplication and HNPP deletion by FISH on stretched chromosome fibers.
    Rautenstrauss B; Fuchs C; Liehr T; Grehl H; Murakami T; Lupski JR
    J Peripher Nerv Syst; 1997; 2(4):319-22. PubMed ID: 10975740
    [No Abstract]   [Full Text] [Related]  

  • 16. Identification of deletion and duplication genotypes of the PMP22 gene using PCR-RFLP, competitive multiplex PCR, and multiplex ligation-dependent probe amplification: a comparison.
    Hung CC; Lee CN; Lin CY; Cheng WF; Chen CA; Hsieh ST; Yang CC; Jong YJ; Su YN; Lin WL
    Electrophoresis; 2008 Feb; 29(3):618-25. PubMed ID: 18200636
    [TBL] [Abstract][Full Text] [Related]  

  • 17. New insights into the biological basis of genomic disorders.
    Myers SR; McCarroll SA
    Nat Genet; 2006 Dec; 38(12):1363-4. PubMed ID: 17133221
    [No Abstract]   [Full Text] [Related]  

  • 18. Genomic rearrangements in inherited disease and cancer.
    Chen JM; Cooper DN; Férec C; Kehrer-Sawatzki H; Patrinos GP
    Semin Cancer Biol; 2010 Aug; 20(4):222-33. PubMed ID: 20541013
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Translocation and gross deletion breakpoints in human inherited disease and cancer I: Nucleotide composition and recombination-associated motifs.
    Abeysinghe SS; Chuzhanova N; Krawczak M; Ball EV; Cooper DN
    Hum Mutat; 2003 Sep; 22(3):229-44. PubMed ID: 12938088
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genome structural variation and sporadic disease traits.
    Lupski JR
    Nat Genet; 2006 Sep; 38(9):974-6. PubMed ID: 16941003
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 15.