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 *

160 related articles for article (PubMed ID: 19516895)

  • 41. Characterization of the human myeloid leukemia-derived cell line GF-D8 by multiplex fluorescence in situ hybridization, subtelomeric probes, and comparative genomic hybridization.
    Tosi S; Giudici G; Rambaldi A; Scherer SW; Bray-Ward P; Dirscherl L; Biondi A; Kearney L
    Genes Chromosomes Cancer; 1999 Mar; 24(3):213-21. PubMed ID: 10451701
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Cryptic chromosomal rearrangement screening in 30 patients with mental retardation and dysmorphic features.
    Rodriguez-Revenga L; Badenas C; Sánchez A; Mallolas J; Carrió A; Pedrinaci S; Barrionuevo JL; Milà M
    Clin Genet; 2004 Jan; 65(1):17-23. PubMed ID: 15032970
    [TBL] [Abstract][Full Text] [Related]  

  • 43. A cryptic t(5;11)(q35;p15.5) in 2 children with acute myeloid leukemia with apparently normal karyotypes, identified by a multiplex fluorescence in situ hybridization telomere assay.
    Brown J; Jawad M; Twigg SR; Saracoglu K; Sauerbrey A; Thomas AE; Eils R; Harbott J; Kearney L
    Blood; 2002 Apr; 99(7):2526-31. PubMed ID: 11895789
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Frequency of truly cryptic subtelomere abnormalities--a study of 534 patients and literature review.
    Yu S; Baker E; Hinton L; Eyre HJ; Waters W; Higgins S; Sutherland GR; Haan E
    Clin Genet; 2005 Nov; 68(5):436-41. PubMed ID: 16207211
    [TBL] [Abstract][Full Text] [Related]  

  • 45. The importance of aneuploidy screening in reciprocal translocation carriers.
    Pujol A; Benet J; Staessen C; Van Assche E; Campillo M; Egozcue J; Navarro J
    Reproduction; 2006 Jun; 131(6):1025-35. PubMed ID: 16735542
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Cryptic chromosome rearrangements detected by subtelomere assay in patients with mental retardation and dysmorphic features.
    Dawson AJ; Putnam S; Schultz J; Riordan D; Prasad C; Greenberg CR; Chodirker BN; Mhanni AA; Chudley AE
    Clin Genet; 2002 Dec; 62(6):488-94. PubMed ID: 12515261
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Multiple fetal anomalies associated with subtle subtelomeric chromosomal rearrangements.
    Souter VL; Glass IA; Chapman DB; Raff ML; Parisi MA; Opheim KE; Disteche CM
    Ultrasound Obstet Gynecol; 2003 Jun; 21(6):609-15. PubMed ID: 12808681
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Prospective screening of patients with unexplained mental retardation using subtelomeric MLPA strongly increases the detection rate of cryptic unbalanced chromosomal rearrangements.
    Stegmann AP; Jonker LM; Engelen JJ
    Eur J Med Genet; 2008; 51(2):93-105. PubMed ID: 18032123
    [TBL] [Abstract][Full Text] [Related]  

  • 49. 18, X, Y aneuploidies and transmission electron microscopy studies in spermatozoa from five carriers of different reciprocal translocations.
    Moretti E; Pascarelli NA; Giannerini V; Geminiani M; Anichini C; Collodel G
    Asian J Androl; 2009 May; 11(3):325-32. PubMed ID: 19349951
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Cryptic terminal chromosome rearrangements in colorectal carcinoma cell lines detected by subtelomeric FISH analysis.
    Stewénius Y; Tanke HJ; Wiegant J; Gisselsson D
    Cytogenet Genome Res; 2006; 114(3-4):257-62. PubMed ID: 16954663
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Del(18p) shown to be a cryptic translocation using a multiprobe FISH assay for subtelomeric chromosome rearrangements.
    Horsley SW; Knight SJ; Nixon J; Huson S; Fitchett M; Boone RA; Hilton-Jones D; Flint J; Kearney L
    J Med Genet; 1998 Sep; 35(9):722-6. PubMed ID: 9733029
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Identification of a subtle t(16;19)(p13.3;p13.3) in an infant with multiple congenital abnormalities using a 12-colour multiplex FISH telomere assay, M-TEL.
    Brown J; Horsley SW; Jung C; Saracoglu K; Janssen B; Brough M; Daschner M; Beedgen B; Kerkhoffs G; Eils R; Harris PC; Jauch A; Kearney L
    Eur J Hum Genet; 2000 Dec; 8(12):903-10. PubMed ID: 11175277
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Submicroscopic terminal deletion of 1p36.3 and Xp23 hidden in complex chromosome rearrangements: independent mechanism of telomere restitution on the two chromatids.
    Reddy KS; Yang X
    Am J Med Genet A; 2003 Mar; 117A(3):261-7. PubMed ID: 12599190
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Cryptic translocation identification in human and mouse using several telomeric multiplex fish (TM-FISH) strategies.
    Henegariu O; Artan S; Greally JM; Chen XN; Korenberg JR; Vance GH; Stubbs L; Bray-Ward P; Ward DC
    Lab Invest; 2001 Apr; 81(4):483-91. PubMed ID: 11304567
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Cryptic translocations involving chromosome 20 in polycythemia vera.
    Busson M; Romana S; Nguyen Khac F; Bernard O; Berger R
    Ann Genet; 2004; 47(4):365-71. PubMed ID: 15581834
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Subtelomeric chromosome aberrations: still a lot to learn.
    Moog U; Arens YH; van Lent-Albrechts JC; Huijts PE; Smeets EE; Schrander-Stumpel CT; Engelen JJ
    Clin Genet; 2005 Nov; 68(5):397-407. PubMed ID: 16207207
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Automated fluorescent genotyping detects 10% of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardation.
    Rio M; Molinari F; Heuertz S; Ozilou C; Gosset P; Raoul O; Cormier-Daire V; Amiel J; Lyonnet S; Le Merrer M; Turleau C; de Blois MC; Prieur M; Romana S; Vekemans M; Munnich A; Colleaux L
    J Med Genet; 2002 Apr; 39(4):266-70. PubMed ID: 11950856
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Preimplantation genetic diagnosis and sperm analysis by fluorescence in-situ hybridization for the most common reciprocal translocation t(11;22).
    Van Assche E; Staessen C; Vegetti W; Bonduelle M; Vandervorst M; Van Steirteghem A; Liebaers I
    Mol Hum Reprod; 1999 Jul; 5(7):682-90. PubMed ID: 10381825
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Cryptic unbalanced translocation t(17;18)(p13.2;q22.3) identified by subtelomeric FISH and defined by array-based comparative genomic hybridization in a patient with mental retardation and dysmorphic features.
    Hwang KS; Pearson MA; Stankiewicz P; Lennon PA; Cooper ML; Wu J; Ou Z; Cai WW; Patel A; Cheung SW
    Am J Med Genet A; 2005 Aug; 137(1):88-93. PubMed ID: 16015583
    [TBL] [Abstract][Full Text] [Related]  

  • 60. An unbalanced half-cryptic translocation involving the 6q subtelomeric region and 2p25.3 in a child with mental retardation: uses and limitations of fluorescence in situ hybridization.
    Batanian JR; Hussain MI
    Clin Genet; 1999 Apr; 55(4):265-8. PubMed ID: 10361988
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.