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 *

207 related articles for article (PubMed ID: 18932219)

  • 1. Molecular and clinical characterization of a recurrent cryptic unbalanced t(4q;18q) resulting in an 18q deletion and 4q duplication.
    Horbinski C; Carter EM; Heard PL; Sathanoori M; Hu J; Vockley J; Gunn S; Hale DE; Surti U; Cody JD
    Am J Med Genet A; 2008 Nov; 146A(22):2898-904. PubMed ID: 18932219
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular characterization of a patient with central nervous system dysmyelination and cryptic unbalanced translocation between chromosomes 4q and 18q.
    Gunn SR; Mohammed M; Reveles XT; Viskochil DH; Palumbos JC; Johnson-Pais TL; Hale DE; Lancaster JL; Hardies LJ; Boespflug-Tanguy O; Cody JD; Leach RJ
    Am J Med Genet A; 2003 Jul; 120A(1):127-35. PubMed ID: 12794705
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Confirmation of a cryptic unbalanced translocation using whole chromosome fluorescence in situ hybridization.
    Mewar R; Kline AD; Jackson L; Overhauser J
    Am J Med Genet; 1992 Nov; 44(4):477-81. PubMed ID: 1442891
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A de novo subterminal trisomy 10p and monosomy 18q in a girl with MCA/MR: case report and review.
    Courtens W; Wuyts W; Scheers S; Van Luijk R; Reyniers E; Rooms L; Ceulemans B; Kooy F; Wauters J
    Eur J Med Genet; 2006; 49(5):402-13. PubMed ID: 16488200
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Another patient with cryptic unbalanced translocation between chromosomes 4q and 18q: evidence by microarray CGH.
    Moncla A; Missirian C; Philip N; Marlin S
    Am J Med Genet A; 2004 Dec; 131(3):314-7. PubMed ID: 15389711
    [No Abstract]   [Full Text] [Related]  

  • 7. Unbalanced three-way chromosomal translocation leading to deletion 18q and duplication 20p.
    Oegema R; van Zutven LJ; van Hassel DA; Huijbregts GC; Hoogeboom AJ
    Eur J Med Genet; 2012 Apr; 55(4):265-8. PubMed ID: 22406089
    [TBL] [Abstract][Full Text] [Related]  

  • 8. New chromosome aberration: duplication of a large part of chromosome 4q and partial deletion of chromosome 1q.
    Merlob P; Kohn G; Litwin A; Nissenkorn I; Katznelson MB; Reisner SH
    Am J Med Genet; 1989 Jan; 32(1):22-6. PubMed ID: 2705479
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Detection of an unbalanced t(4;15) by FISH in a child with multiple congenital anomalies.
    Celep F; Acar H; Aynaci O; Aynaci FM; Karagüzel A
    Genet Couns; 2001; 12(4):319-26. PubMed ID: 11837600
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Jumping translocation in a newborn boy with dup(4q) and severe hydrops fetalis.
    Duval E; van den Enden A; Vanhaesebrouck P; Speleman F
    Am J Med Genet; 1994 Aug; 52(2):214-7. PubMed ID: 7802011
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A patient with isochromosome 18q, radial-thumb aplasia, thrombocytopenia, and an unbalanced 10;18 chromosome translocation.
    Sahoo T; Naeem R; Pham K; Chheng S; Noblin ST; Bacino CA; Gambello MJ
    Am J Med Genet A; 2005 Feb; 133A(1):93-8. PubMed ID: 15637724
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Maternal balanced translocation leading to partial duplication of 4q and partial deletion of 1p in a son: cytogenetic and FISH studies using band-specific painting probes generated by chromosome microdissection.
    Chen Z; Grebe TA; Guan XY; Notohamiprodjo M; Nutting PJ; Stone JF; Trent JM; Sandberg AA
    Am J Med Genet; 1997 Aug; 71(2):160-6. PubMed ID: 9217215
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Co-existence of 9p deletion and Silver-Russell syndromes in a patient with maternally inherited cryptic complex chromosome rearrangement involving chromosomes 4, 9, and 11.
    Hu J; Sathanoori M; Kochmar S; Madan-Khetarpal S; McGuire M; Surti U
    Am J Med Genet A; 2013 Jan; 161A(1):179-84. PubMed ID: 23225375
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Complex Rearrangement Involving Three Chromosomes, Four Breakpoints and a 2.7-Mb Deletion in the 18q Segment Observed in a Girl with Mild Learning Difficulties.
    Kontodiou M; Daskalakis G; Vetro A; Paspaliaris V; Papaioannou G; Dagklis T; Tsakiridis I; Ziegler M; Liehr T; Thomaidis L; Papoulidis I; Manolakos E
    Cytogenet Genome Res; 2015; 147(2-3):118-23. PubMed ID: 26681178
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mapping susceptibility gene locus for IgA deficiency at del(18)(q22.3-q23); report of familial cryptic chromosome t(18q; 10p) translocations.
    Dostal A; Linnankivi T; Somer M; Kähkönen M; Litzman J; Tienari P
    Int J Immunogenet; 2007 Jun; 34(3):143-7. PubMed ID: 17504501
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Array-based comparative genomic hybridization facilitates identification of breakpoints of a novel der(1)t(1;18)(p36.3;q23)dn in a child presenting with mental retardation.
    Lennon PA; Cooper ML; Curtis MA; Lim C; Ou Z; Patel A; Cheung SW; Bacino CA
    Am J Med Genet A; 2006 Jun; 140(11):1156-63. PubMed ID: 16688748
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular cytogenetic characterization of a 2q35-q37 duplication and a 4q35.1-q35.2 deletion in two cousins: a genotype-phenotype analysis.
    Ronzoni L; Peron A; Bianchi V; Baccarin M; Guerneri S; Silipigni R; Lalatta F; Bedeschi MF
    Am J Med Genet A; 2015 Jul; 167(7):1551-9. PubMed ID: 25851921
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular characterization of distal 4q duplication in two patients using oligonucleotide array-based comparative genomic hybridization (oaCGH) analysis.
    Thapa M; Asamoah A; Gowans GC; Platky KC; Barch MJ; Mouchrani P; Rajakaruna C; Hersh JH
    Am J Med Genet A; 2014 Apr; 164A(4):1069-74. PubMed ID: 24459084
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Detection of cryptic chromosome aberrations in a patient with a balanced t(1;9)(p34.2;p24) by array-based comparative genomic hybridization.
    Hayashi S; Kurosawa K; Imoto I; Mizutani S; Inazawa J
    Am J Med Genet A; 2005 Nov; 139(1):32-6. PubMed ID: 16222686
    [TBL] [Abstract][Full Text] [Related]  

  • 20. High resolution genomic analysis of 18q- using oligo-microarray comparative genomic hybridization (aCGH).
    Heard PL; Carter EM; Crandall AC; Sebold C; Hale DE; Cody JD
    Am J Med Genet A; 2009 Jul; 149A(7):1431-7. PubMed ID: 19533772
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.