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 *

210 related articles for article (PubMed ID: 11092830)

  • 1. Molecular mechanisms for constitutional chromosomal rearrangements in humans.
    Shaffer LG; Lupski JR
    Annu Rev Genet; 2000; 34():297-329. PubMed ID: 11092830
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Is there an association with constitutional structural chromosomal abnormalities and hematologic neoplastic process? A short review.
    Panani AD
    Ann Hematol; 2009 Apr; 88(4):293-9. PubMed ID: 19129995
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.
    Caliskan MO; Karauzum SB; Mihci E; Tacoy S; Luleci G
    Genet Couns; 2005; 16(2):129-38. PubMed ID: 16080292
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Implications of human genome architecture for rearrangement-based disorders: the genomic basis of disease.
    Shaw CJ; Lupski JR
    Hum Mol Genet; 2004 Apr; 13 Spec No 1():R57-64. PubMed ID: 14764619
    [TBL] [Abstract][Full Text] [Related]  

  • 5. What have studies of genomic disorders taught us about our genome?
    Simmons AD; Carvalho CM; Lupski JR
    Methods Mol Biol; 2012; 838():1-27. PubMed ID: 22228005
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cryptic genomic imbalances in de novo and inherited apparently balanced chromosomal rearrangements: array CGH study of 47 unrelated cases.
    Schluth-Bolard C; Delobel B; Sanlaville D; Boute O; Cuisset JM; Sukno S; Labalme A; Duban-Bedu B; Plessis G; Jaillard S; Dubourg C; Henry C; Lucas J; Odent S; Pasquier L; Copin H; Latour P; Cordier MP; Nadeau G; Till M; Edery P; Andrieux J
    Eur J Med Genet; 2009; 52(5):291-6. PubMed ID: 19505601
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Role of cytogenetics and molecular cytogenetics in the diagnosis of genetic imbalances.
    Dave BJ; Sanger WG
    Semin Pediatr Neurol; 2007 Mar; 14(1):2-6. PubMed ID: 17331878
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Acquired chromosomal rearrangements targeting selected transcription factors: contribution of molecular cytogenetic and expression analyses to the identification of clinically and biologically relevant subgroups in hematological malignancies.
    Poppe B; De Paepe A; Speleman F
    Verh K Acad Geneeskd Belg; 2007; 69(1):47-64. PubMed ID: 17427874
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Submicroscopic terminal deletions and duplications in retarded patients with unclassified malformation syndromes.
    Riegel M; Baumer A; Jamar M; Delbecque K; Herens C; Verloes A; Schinzel A
    Hum Genet; 2001 Sep; 109(3):286-94. PubMed ID: 11702209
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular mechanisms for genomic disorders.
    Inoue K; Lupski JR
    Annu Rev Genomics Hum Genet; 2002; 3():199-242. PubMed ID: 12142364
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Chromosome abnormalities in human beings.
    McFadden DE; Friedman JM
    Mutat Res; 1997 Dec; 396(1-2):129-40. PubMed ID: 9434864
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular mechanism for duplication 17p11.2- the homologous recombination reciprocal of the Smith-Magenis microdeletion.
    Potocki L; Chen KS; Park SS; Osterholm DE; Withers MA; Kimonis V; Summers AM; Meschino WS; Anyane-Yeboa K; Kashork CD; Shaffer LG; Lupski JR
    Nat Genet; 2000 Jan; 24(1):84-7. PubMed ID: 10615134
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Rapid detection of submicroscopic chromosomal rearrangements in children with multiple congenital anomalies using high density oligonucleotide arrays.
    Ming JE; Geiger E; James AC; Ciprero KL; Nimmakayalu M; Zhang Y; Huang A; Vaddi M; Rappaport E; Zackai EH; Shaikh TH
    Hum Mutat; 2006 May; 27(5):467-73. PubMed ID: 16619270
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular cytogenetic characterization of a constitutional complex intrachromosomal 4q rearrangement in a patient with multiple congenital anomalies.
    Thienpont B; Gewillig M; Fryns JP; Devriendt K; Vermeesch J
    Cytogenet Genome Res; 2006; 114(3-4):338-41. PubMed ID: 16954676
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Complex chromosomal rearrangements: origin and meiotic behavior.
    Pellestor F; Anahory T; Lefort G; Puechberty J; Liehr T; Hédon B; Sarda P
    Hum Reprod Update; 2011; 17(4):476-94. PubMed ID: 21486858
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Contribution of molecular cytogenetics in the diagnosis of chromosomal abnormalities].
    Bouayed Abdelmoula N
    Ann Biol Clin (Paris); 2004; 62(6):629-37. PubMed ID: 15563421
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Constitutional chromosome aberrations as pathogenetic events in hematologic malignancies.
    Welborn J
    Cancer Genet Cytogenet; 2004 Mar; 149(2):137-53. PubMed ID: 15036890
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A cytogeneticist's perspective on genomic microarrays.
    Shaffer LG; Bejjani BA
    Hum Reprod Update; 2004; 10(3):221-6. PubMed ID: 15140869
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A 5q12.1-5q12.3 microdeletion in a case with a balanced exceptional complex chromosomal rearrangement.
    Cetin Z; Yakut S; Clark OA; Mihci E; Berker S; Luleci G
    Gene; 2013 Mar; 516(1):176-80. PubMed ID: 23262338
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Identification of the breakpoint-flanking markers on chromosomes 1 and 17 of a constitutional translocation T(1;17)(P36;Q12-21) in a patient with neuroblastoma].
    Laureys GG
    Verh K Acad Geneeskd Belg; 1995; 57(5):389-422. PubMed ID: 8571670
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.