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 *

201 related articles for article (PubMed ID: 3610150)

  • 21. Interstitial deletion of the long arm of chromosome 2: a clinically recognizable microdeletion syndrome?
    Maas SM; Hoovers JM; van Seggelen ME; Menzel DM; Hennekam RC
    Clin Dysmorphol; 2000 Jan; 9(1):47-53. PubMed ID: 10649798
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Deletions in chromosome 2 and fragile sites.
    Palmer CG; Heerema N; Bull M
    Am J Med Genet; 1990 Jun; 36(2):214-8. PubMed ID: 2368809
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Deletion of chromosome 3q proximal region gives rise to a variable phenotype.
    Mackie Ogilvie C; Rooney SC; Hodgson SV; Berry AC
    Clin Genet; 1998 Mar; 53(3):220-2. PubMed ID: 9630079
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Definition of a small chromosomal rearrangement on chromosome 11p14 by molecular cytogenetics in situ hybridization.
    Bérubé D; Gagné R
    Clin Invest Med; 1992 Dec; 15(6):489-93. PubMed ID: 1286530
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A folate sensitive heritable fragile site at 19p13.
    Tommerup N; Nielsen J; Mikkelsen M
    Clin Genet; 1985 May; 27(5):510-4. PubMed ID: 3159519
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Two different structural abnormalities of chromosome 13 in offspring of chromosomally normal parents with two fragile sites.
    Mules EH; Stamberg J; Jabs EW; Leonard CO
    Clin Genet; 1983 May; 23(5):380-5. PubMed ID: 6851231
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Duplication 11q and deletion 5p syndromes due to a reciprocal translocation segregating in four generations.
    Mutchinick O; Ramos Z; Sánchez F; Ruz L; Lisker R; Ovseyevitz J
    Am J Med Genet; 1988 Jan; 29(1):187-92. PubMed ID: 3344767
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Molecular detection of a translocation (Y;11) (q11.2;q24) in a 45,X male with signs of Jacobsen syndrome.
    Van Hemel JO; Eussen B; Wesby-van Swaay E; Oostra BA
    Hum Genet; 1992 Mar; 88(6):661-7. PubMed ID: 1551671
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Expression of fragile sites in human sperm and lymphocyte chromosomes.
    Benet J; Fuster C; Genescà A; Navarro J; Miró R; Egozcue J; Templado C
    Hum Genet; 1989 Feb; 81(3):239-42. PubMed ID: 2921032
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Folate-sensitive fragile sites in Chinese hamster cell lines.
    Simi S; Vatteroni L; Piras A; Mariani T; Rainaldi G
    Cancer Genet Cytogenet; 1990 Jun; 46(2):209-16. PubMed ID: 2340492
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Assignment of the apolipoprotein A-I gene to 11q23 based on RFLP in a case with a partial deletion of chromosome 11, del(11)(q23.3----qter).
    Arinami T; Hirano T; Kobayashi K; Yamanouchi Y; Hamaguchi H
    Hum Genet; 1990 Jun; 85(1):39-40. PubMed ID: 1972696
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Noninvolvement of chromosome 16 in karyotype evolution of acute myeloid leukemia in a patient with a heritable fragile site on 16q22.
    Haas OA; Nacheva E; Schwarzmeier JD
    Cancer Genet Cytogenet; 1985 May; 17(1):1-12. PubMed ID: 3857107
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Detection of a 15q deletion in a child with Angelman syndrome by cytogenetic analysis and flow cytometry.
    Cooke A; Tolmie JL; Glencross FJ; Boyd E; Clarke MM; Day R; Stephenson JB; Connor JM
    Am J Med Genet; 1989 Apr; 32(4):545-9. PubMed ID: 2774001
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Partial deletion of 14q and partial duplication of 14q in sibs: testicular mosaicism for t(14q;14q) as a common mechanism.
    Masada CT; Olney AH; Fordyce R; Sanger WG
    Am J Med Genet; 1989 Dec; 34(4):528-34. PubMed ID: 2624263
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A new case of familial paracentric inversion of chromosome 2.
    Donti E; Rosetti A; Carloni I; Venti Donti G
    Hum Genet; 1987 Feb; 75(2):195. PubMed ID: 3817813
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Interstitial deletion of the long arm of chromosome 11 determined by fluorescence in situ hybridization.
    Hori T; Masuno M; Wakazono A; Takahashi E; Katakura R; Orii T
    Jpn J Hum Genet; 1993 Jun; 38(2):219-24. PubMed ID: 8358045
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Expression of folate sensitive and aphidicolin induced chromosomal fragile sites in familial neuroblastoma.
    Ankathil R; Kusumakumary P; Priyakumary T; Krishnan Nair M
    J Exp Clin Cancer Res; 2002 Sep; 21(3):383-8. PubMed ID: 12385582
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Noninvolvement of a constitutional heritable fragile site at 10q24.2 in rearranged chromosomes from rectal carcinoma cells.
    Muleris M; Dutrillaux AM; Lombard M; Dutrillaux B
    Cancer Genet Cytogenet; 1987 Mar; 25(1):7-13. PubMed ID: 3467833
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Localization of fragile sites in the karyotype of Sus scrofa domestica: present status.
    Rønne M
    Hereditas; 1995; 122(2):153-62. PubMed ID: 7558883
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Double chromosome anomaly: interstitial deletion 5q and reciprocal translocation (1;11)(p22;q21).
    de Michelena MI; Villacorta J; Chávez J
    Am J Med Genet; 1990 May; 36(1):29-32. PubMed ID: 2185634
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.