BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

259 related articles for article (PubMed ID: 15741672)

  • 1. Recombination aneusomy of subtelomeric regions of chromosome 5, resulting from a large familial pericentric inversion inv(5)(p15.33q35.3).
    Bocian E; Suchenek K; Obersztyn E; Nowakowska B; Mazurczak T
    J Appl Genet; 2005; 46(1):109-14. PubMed ID: 15741672
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Familial pericentric inversion of chromosome 18: intrafamilial variability of the recombinant dup(18q).
    Prontera P; Buldrini B; Aiello V; Rogaia D; Mencarelli A; Gruppioni R; Bonfatti A; Beltrami N; Donti E; Sensi A
    Genet Couns; 2010; 21(1):91-7. PubMed ID: 20420035
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Duplication of 11p14.3-p15.1 in a mentally retarded proband and his mother detected by G-banding and confirmed by high-resolution CGH and BAC FISH.
    Wyandt HE; Shim SH; Mark HF; Huang XL; Milunsky JM
    Exp Mol Pathol; 2006 Jun; 80(3):262-6. PubMed ID: 16516886
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Relatives with opposite chromosome constitutions, rec(10)dup(10p)inv(10)(p15.1q26.12) and rec(10)dup(10q)inv(10)(p15.1q26.12), due to a familial pericentric inversion.
    Ciuladaite Z; Preiksaitiene E; Utkus A; Kučinskas V
    Cytogenet Genome Res; 2014; 144(2):109-13. PubMed ID: 25401700
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial pericentric inversion of chromosome 18: behavioral abnormalities in patients heterozygous for either the dup(18p)/del(18q) or dup(18q)/del(18p) recombinant chromosome.
    Vermeulen SJ; Speleman F; Vanransbeeck L; Verspeet J; Menten B; Verschraegen-Spae MR; Wilde PD; Messiaen L; Michaelis RC; Leroy JG
    Eur J Hum Genet; 2005 Jan; 13(1):52-8. PubMed ID: 15470365
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Pericentric inversion of chromosome 4 giving rise to dup(4p) and dup(4q) recombinants within a single kindred.
    Hirsch B; Baldinger S
    Am J Med Genet; 1993 Jan; 45(1):5-8. PubMed ID: 8418660
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A variant Cri du Chat phenotype and autism spectrum disorder in a subject with de novo cryptic microdeletions involving 5p15.2 and 3p24.3-25 detected using whole genomic array CGH.
    Harvard C; Malenfant P; Koochek M; Creighton S; Mickelson EC; Holden JJ; Lewis ME; Rajcan-Separovic E
    Clin Genet; 2005 Apr; 67(4):341-51. PubMed ID: 15733271
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Monosomy 19pter and trisomy 19q13-qter in two siblings arising from a maternal pericentric inversion: clinical data and molecular characterization.
    Schluth-Bolard C; Till M; Rafat A; Labalme A; Le Lorc'h M; Banquart E; Angei C; Cordier MP; Romana SP; Edery P; Sanlaville D
    Eur J Med Genet; 2008; 51(6):622-30. PubMed ID: 18674648
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Distinct dysmorphic syndrome in a child with inverted distal 5q duplication.
    Fryns JP; Kleczkowska A; Borghgraef M; Raveschot J; Van den Berghe H
    Ann Genet; 1987; 30(3):186-8. PubMed ID: 3499858
    [TBL] [Abstract][Full Text] [Related]  

  • 10. High recurrence of recombinants in a family with pericentric inversion of chromosome 18.
    Mejía-Baltodano G; Bobadilla L; Gonzalez RM; Barros-Núñez P
    Ann Genet; 1997; 40(3):164-8. PubMed ID: 9401106
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Recombinant 4 syndrome due to an unbalanced pericentric inversion of chromosome 4.
    Battaglia A; Brothman AR; Carey JC
    Am J Med Genet; 2002 Sep; 112(1):103-6. PubMed ID: 12239731
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Familial pericentric inversion of chromosome 8.
    Sujansky E; Smith AC; Peakman DC; McConnell TS; Baca P; Robinson A
    Am J Med Genet; 1981; 10(3):229-35. PubMed ID: 6171164
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Two complementary recombinant chromosomes 5 in a healthy woman.
    Bartsch O; Ergun MA; Balci S; Kan D; Eggermann T; Kotzot D
    Cytogenet Genome Res; 2006; 114(2):178-82. PubMed ID: 16825772
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Partial monosomy 5p and partial trisomy 5q due to paternal pericentric inversion 5(p15.1q35.1).
    Sonoda T; Kawaguchi K; Ohba K; Madokoro H; Ohdo S
    Jinrui Idengaku Zasshi; 1989 Jun; 34(2):129-34. PubMed ID: 2671452
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Partial monosomy 5p and partial trisomy 5q due to paternal pericentric inversion of chromosome 5.
    Ono K; Ohashi Y; Nakano H; Togashi H; Kannari Y; Isono S
    Jpn J Hum Genet; 1993 Sep; 38(3):319-28. PubMed ID: 8260723
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A fourteen years follow-up of a case of partial trisomy 12q and monosomy 12p recombinants of a familial pericentric inversion of chromosome 12: clinical, cytogenetic and molecular observations.
    Vaglio A; Milunsky A; Huang XL; Quadrelli A; Mechoso B; Quadrelli R
    Eur J Med Genet; 2007; 50(3):224-32. PubMed ID: 17329177
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The Wolf-Hirschhorn syndrome in adulthood: evaluation of a 24-year-old man with a rec(4) chromosome.
    Ogle R; Sillence DO; Merrick A; Ell J; Lo B; Robson L; Smith A
    Am J Med Genet; 1996 Oct; 65(2):124-7. PubMed ID: 8911603
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Unexpected identification of two interstitial deletions in a patient with a pericentric inversion of a chromosome 4 and an abnormal phenotype.
    Piovani G; Borsani G; Bertini V; Kalscheuer VM; Viertel P; Bellotti D; Valseriati D; Barlati S
    Eur J Med Genet; 2006; 49(3):215-23. PubMed ID: 16762823
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Familial 10p trisomy resulting from a maternal pericentric inversion.
    Kozma C; Meck JM
    Am J Med Genet; 1994 Feb; 49(3):281-7. PubMed ID: 8209887
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A familial complex chromosome translocation resulting in duplication of 6p25.
    Vermeesch JR; Thoelen R; Fryns JP
    Ann Genet; 2004; 47(3):275-80. PubMed ID: 15337473
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.