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 *

99 related articles for article (PubMed ID: 12746414)

  • 1. Multicolour FISH fine mapping unravels an insertion as a complex chromosomal rearrangement involving six breakpoints and a 5.89 Mb large deletion.
    Kraus J; Cohen M; Speicher MR
    J Med Genet; 2003 May; 40(5):e60. PubMed ID: 12746414
    [No Abstract]   [Full Text] [Related]  

  • 2. Molecular cytogenetic analysis of complex chromosomal rearrangements in patients with mental retardation and congenital malformations: delineation of 7q21.11 breakpoints.
    Vermeulen S; Menten B; Van Roy N; Van Limbergen H; De Paepe A; Mortier G; Speleman F
    Am J Med Genet A; 2004 Jan; 124A(1):10-8. PubMed ID: 14679581
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mild Wolf-Hirschhorn syndrome: micro-array CGH analysis of atypical 4p16.3 deletions enables refinement of the genotype-phenotype map.
    Van Buggenhout G; Melotte C; Dutta B; Froyen G; Van Hummelen P; Marynen P; Matthijs G; de Ravel T; Devriendt K; Fryns JP; Vermeesch JR
    J Med Genet; 2004 Sep; 41(9):691-8. PubMed ID: 15342700
    [No Abstract]   [Full Text] [Related]  

  • 4. Mosaicism for a dup(12)(q22q13) in a patient with hypomelanosis of Ito and asymmetry.
    Schmidt H; Uhrig S; Lederer G; Murken J; Speicher MR; Schuffenhauer S
    J Med Genet; 2000 Oct; 37(10):804-7. PubMed ID: 11183189
    [No Abstract]   [Full Text] [Related]  

  • 5. FISH-microdissection (FISH-MD) analysis of complex chromosome rearrangements.
    Weimer J; Kiechle M; Arnold N
    Cytogenet Cell Genet; 2000; 88(1-2):114-8. PubMed ID: 10773683
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Delineation of a 2.2 Mb microdeletion at 5q35 associated with microcephaly and congenital heart disease.
    Baekvad-Hansen M; Tümer Z; Delicado A; Erdogan F; Tommerup N; Larsen LA
    Am J Med Genet A; 2006 Mar; 140(5):427-33. PubMed ID: 16470726
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Improved definition of chromosomal breakpoints using high-resolution multicolour banding.
    Lemke J; Chudoba I; Senger G; Stumm M; Loncarevic IF; Henry C; Zabel B; Claussen U
    Hum Genet; 2001 Jun; 108(6):478-83. PubMed ID: 11499672
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1.
    Devriendt K; Matthijs G; Van Dael R; Gewillig M; Eyskens B; Hjalgrim H; Dolmer B; McGaughran J; Bröndum-Nielsen K; Marynen P; Fryns JP; Vermeesch JR
    Am J Hum Genet; 1999 Apr; 64(4):1119-26. PubMed ID: 10090897
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Characterization of an interstitial 4q32 deletion in a patient with mental retardation and a complex chromosome rearrangement.
    Tzschach A; Menzel C; Erdogan F; Istifli ES; Rieger M; Ovens-Raeder A; Macke A; Ropers HH; Ullmann R; Kalscheuer V
    Am J Med Genet A; 2010 Apr; 152A(4):1008-12. PubMed ID: 20358617
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Phenotypic variability of a deletion and duplication 6q16.1 → q21 due to a paternal balanced ins(7;6)(p15;q16.1q21).
    Spreiz A; Müller D; Zotter S; Albrecht U; Baumann M; Fauth C; Erdel M; Zschocke J; Utermann G; Kotzot D
    Am J Med Genet A; 2010 Nov; 152A(11):2762-7. PubMed ID: 20954245
    [TBL] [Abstract][Full Text] [Related]  

  • 11. An exceptional complex chromosomal rearrangement (CCR) with eight breakpoints involving four chromosomes (1;3;9;14) in an azoospermic male with normal phenotype.
    Bartels I; Starke H; Argyriou L; Sauter SM; Zoll B; Liehr T
    Eur J Med Genet; 2007; 50(2):133-8. PubMed ID: 17174164
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Systematic screening at diagnosis of -5/del(5)(q31), -7, or chromosome 8 aneuploidy by interphase fluorescence in situ hybridization in 110 acute myelocytic leukemia and high-risk myelodysplastic syndrome patients: concordances and discrepancies with conventional cytogenetics.
    Beyer V; Castagné C; Mühlematter D; Parlier V; Gmür J; Hess U; Kovacsovics T; Meyer-Monard S; Tichelli A; Tobler A; Jacky E; Schanz U; Bargetzi M; Hagemeijer A; de Witte T; van Melle G; Jotterand M
    Cancer Genet Cytogenet; 2004 Jul; 152(1):29-41. PubMed ID: 15193439
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genotype-phenotype correlation of 5p-syndrome: pitfall of diagnosis.
    Kondoh T; Shimokawa O; Harada N; Doi T; Yun C; Gohda Y; Kinoshita F; Matsumoto T; Moriuchi H
    J Hum Genet; 2005; 50(1):26-29. PubMed ID: 15602631
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Characterization of terminal deletions at 7q32 and 22q13.3 healed by De novo telomere addition.
    Varley H; Di S; Scherer SW; Royle NJ
    Am J Hum Genet; 2000 Sep; 67(3):610-22. PubMed ID: 10924407
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Familial pericentric inversion of chromosome 5 in a family with benign neonatal convulsions.
    Concolino D; Iembo MA; Rossi E; Giglio S; Coppola G; Miraglia Del Giudice E; Strisciuglio P
    J Med Genet; 2002 Mar; 39(3):214-6. PubMed ID: 11897828
    [No Abstract]   [Full Text] [Related]  

  • 16. Heterogeneity of the 7q36 breakpoints in the t(7;12) involving ETV6 in infant leukemia.
    Tosi S; Hughes J; Scherer SW; Nakabayashi K; Harbott J; Haas OA; Cazzaniga G; Biondi A; Kempski H; Kearney L
    Genes Chromosomes Cancer; 2003 Oct; 38(2):191-200. PubMed ID: 12939747
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular characterisation of a mosaicism with a complex chromosome rearrangement: evidence for coincident chromosome healing by telomere capture and neo-telomere formation.
    Chabchoub E; Rodríguez L; Galán E; Mansilla E; Martínez-Fernandez ML; Martínez-Frías ML; Fryns JP; Vermeesch JR
    J Med Genet; 2007 Apr; 44(4):250-6. PubMed ID: 17172463
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular analysis of a constitutional complex genome rearrangement with 11 breakpoints involving chromosomes 3, 11, 12, and 21 and a approximately 0.5-Mb submicroscopic deletion in a patient with mild mental retardation.
    Borg K; Stankiewicz P; Bocian E; Kruczek A; Obersztyn E; Lupski JR; Mazurczak T
    Hum Genet; 2005 Nov; 118(2):267-75. PubMed ID: 16160854
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal diagnosis of 2q32 deletion syndrome characterized by multiple segmental deletions and complex chromosomal rearrangement involving chromosomes 2, 5 and 7.
    Thorson HL; Surti U; Sathanoori M; Kochmar SJ; Torchia B; Rajkovic A
    Fetal Diagn Ther; 2012; 31(3):196-200. PubMed ID: 22415219
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Fine-mapping of cytogenetically undetectable EWS/ERG fusions on DNA fibers of Ewing tumors.
    Hattinger CM; Rumpler S; Kovar H; Ambros PF
    Cytogenet Cell Genet; 2001; 93(1-2):29-35. PubMed ID: 11474174
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.