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 *

116 related articles for article (PubMed ID: 21434829)

  • 41. Comparative genomic hybridization-array analysis enhances the detection of aneuploidies and submicroscopic imbalances in spontaneous miscarriages.
    Schaeffer AJ; Chung J; Heretis K; Wong A; Ledbetter DH; Lese Martin C
    Am J Hum Genet; 2004 Jun; 74(6):1168-74. PubMed ID: 15127362
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Duplication of chromosome region 8p23.1-->p23.3: a benign variant?
    Engelen JJ; Moog U; Evers JL; Dassen H; Albrechts JC; Hamers AJ
    Am J Med Genet; 2000 Mar; 91(1):18-21. PubMed ID: 10751083
    [TBL] [Abstract][Full Text] [Related]  

  • 43. A new chromosome 9 variant: an extra band within the 9qh region.
    Hoo JJ
    Clin Genet; 1992 Mar; 41(3):157-8. PubMed ID: 1563090
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Application of a target array comparative genomic hybridization to prenatal diagnosis.
    Park JH; Woo JH; Shim SH; Yang SJ; Choi YM; Yang KS; Cha DH
    BMC Med Genet; 2010 Jun; 11():102. PubMed ID: 20576126
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Prenatal detection of de novo inversion of chromosome 9 with duplicated heterochromatic region and postnatal follow-up.
    Kim JJ; Rhee HS; Chung YT; Park SY; Choi SK
    Exp Mol Med; 1999 Sep; 31(3):134-6. PubMed ID: 10551261
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Identification of recurrent chromosomal breakpoints in multiple myeloma with complex karyotypes by combined G-banding, spectral karyotyping, and fluorescence in situ hybridization analyses.
    Sáez B; Martín-Subero JI; Largo C; Martín MC; Odero MD; Prosper F; Siebert R; Calasanz MJ; Cigudosa JC
    Cancer Genet Cytogenet; 2006 Sep; 169(2):143-9. PubMed ID: 16938572
    [TBL] [Abstract][Full Text] [Related]  

  • 47. BAC CGH-array identified specific small-scale genomic imbalances in diploid DMBA-induced rat mammary tumors.
    Samuelson E; Karlsson S; Partheen K; Nilsson S; Szpirer C; Behboudi A
    BMC Cancer; 2012 Aug; 12():352. PubMed ID: 22894538
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Chromosomal aberrations evaluated by CGH, FISH and GTG-banding in a case of AIDS-related Burkitt's lymphoma.
    Zunino A; Viaggi S; Ottaggio L; Fronza G; Schenone A; Roncella S; Abbondandolo A
    Haematologica; 2000 Mar; 85(3):250-5. PubMed ID: 10702812
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Duplication of euchromatin without phenotypic effects: a variant of chromosome 16.
    Bryke CR; Breg WR; Potluri VR; Yang-Feng TL
    Am J Med Genet; 1990 May; 36(1):43-4. PubMed ID: 2333906
    [TBL] [Abstract][Full Text] [Related]  

  • 50. [Genomic abnormalities in children with mental retardation and autism: the use of comparative genomic hybridization in situ (HRCGH) and molecular karyotyping with DNA-microchips (array CGH)].
    Vorsanova SG; Iurov IIu; Kurinnaia OS; Voinova VIu; Iurov IuB
    Zh Nevrol Psikhiatr Im S S Korsakova; 2013; 113(8):46-9. PubMed ID: 24077551
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Prenatal diagnosis in the presence of an extra small chromosome in amniotic cell culture.
    Chen H; Harris J
    Ann Genet; 1980; 23(2):97-9. PubMed ID: 6967293
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Duplication of 8p23.1: a cytogenetic anomaly with no established clinical significance.
    Barber JC; Joyce CA; Collinson MN; Nicholson JC; Willatt LR; Dyson HM; Bateman MS; Green AJ; Yates JR; Dennis NR
    J Med Genet; 1998 Jun; 35(6):491-6. PubMed ID: 9643291
    [TBL] [Abstract][Full Text] [Related]  

  • 53. A Novel Variant Rearrangement of the Rare Aberration dic(17;20)(p11.2;q11.2) Characterized by Array-CGH as an Insertion in a Patient with Myelodysplastic Syndrome of Multilineage Dysplasia (MDS-MLD).
    Vazmitsel MA; Grammatopoulou V; Yao J; Batanian JR
    Cytogenet Genome Res; 2020; 160(1):22-28. PubMed ID: 32018267
    [TBL] [Abstract][Full Text] [Related]  

  • 54. [Heteromorphism of chromosome 1, 9 and 16 homologs in persons living in regions differing in the level of longevity].
    Kuznetsova SM; Zaritskaia MIu; Berdyshev GD
    Tsitol Genet; 1988; 22(4):27-32. PubMed ID: 2973673
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Integration of microarray analysis into the clinical diagnosis of hematological malignancies: How much can we improve cytogenetic testing?
    Peterson JF; Aggarwal N; Smith CA; Gollin SM; Surti U; Rajkovic A; Swerdlow SH; Yatsenko SA
    Oncotarget; 2015 Aug; 6(22):18845-62. PubMed ID: 26299921
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Prenatal diagnosis of a familial complex chromosomal rearrangement involving chromosomes 5, 10, 16 and 18.
    Lee MH; Park SY; Kim YM; Kim JM; Han JY; Kim MY; Ryu HM
    Prenat Diagn; 2002 Feb; 22(2):102-4. PubMed ID: 11857612
    [TBL] [Abstract][Full Text] [Related]  

  • 57. [Clinical and genetic analysis of a boy with 9q34.3 microdeletion syndrome].
    Wu D; Li T; Wang H; Shi W; Hou Q; Zhang H; Wang T; Yang Y; Liao S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Dec; 34(6):849-852. PubMed ID: 29188614
    [TBL] [Abstract][Full Text] [Related]  

  • 58. [The biochemical marker dynamics of the maternal serum in different chromosomal disorders of the fetus].
    Arbuzova SB; Nikolenko MI; Khlevnaia LA; Fedotova OO; Solov'eva VD; Malova SA; Krasnov AV
    Tsitol Genet; 1998; 32(5):75-9. PubMed ID: 9879118
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Genomic characterization of prenatally detected chromosomal structural abnormalities using oligonucleotide array comparative genomic hybridization.
    Li P; Pomianowski P; DiMaio MS; Florio JR; Rossi MR; Xiang B; Xu F; Yang H; Geng Q; Xie J; Mahoney MJ
    Am J Med Genet A; 2011 Jul; 155A(7):1605-15. PubMed ID: 21671377
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Spectral karyotyping and fluorescence in situ hybridization detect novel chromosomal aberrations, a recurring involvement of chromosome 21 and amplification of the MYC oncogene in acute myeloid leukaemia M2.
    Hilgenfeld E; Padilla-Nash H; McNeil N; Knutsen T; Montagna C; Tchinda J; Horst J; Ludwig WD; Serve H; Büchner T; Berdel WE; Schröck E; Ried T
    Br J Haematol; 2001 May; 113(2):305-17. PubMed ID: 11380393
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.