BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

789 related articles for article (PubMed ID: 17515297)

  • 41. Partial trisomy 8p (8p11.2-->pTER) and deletion of 13q (13q32-->qTER): case report.
    Yeşilyurt A; Dilli D; Oguz S; Dilmen U; Altug N; Candemir Z
    Genet Couns; 2011; 22(1):35-40. PubMed ID: 21614986
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Temtamy-like syndrome associated with translocation of 2p24 and 9q32.
    Talisetti A; Forrester SR; Gregory D; Johnson L; Schneider MC; Kimonis VE
    Clin Dysmorphol; 2003 Jul; 12(3):175-7. PubMed ID: 14564155
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Molecular and cytogenetic characterization of a recurrent unbalanced translocation (4;21)(p16.3;q22.1): relevance to the Wolf-Hirschhorn and Down syndrome critical regions.
    Sebastio G; Perone L; Guzzetta V; Sebastio L; Vicari L; Della Casa R; Gurrieri F; Zappata S; Pomponi MG; Mazzei A; Neri G; Andria G; Brahe C
    Am J Med Genet; 1996 May; 63(2):366-72. PubMed ID: 8725787
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Partial trisomy 1q (1q32-->1qter) in adulthood: further delineation of the phenotype.
    Van Buggenhout G; De Coen L; Fryns JP
    Ann Genet; 1998; 41(2):77-81. PubMed ID: 9706337
    [TBL] [Abstract][Full Text] [Related]  

  • 45. "Essentially pure" partial trisomy (6)(p23-->pter) in two brothers due to maternal t(6;17)(p23;p13.3).
    Röthlisberger B; Kotzot D; Gnehm HE; Schinzel A
    Am J Med Genet; 1999 Aug; 85(4):389-94. PubMed ID: 10398266
    [TBL] [Abstract][Full Text] [Related]  

  • 46. An unusual clinical characterization of a male with distal partial trisomy 1q42.1 and monosomy 4q35.1 and review of the literature.
    Wang CB; Lin SP; Chen CP; Chen YJ; Lee CC
    Genet Couns; 2006; 17(4):435-40. PubMed ID: 17375530
    [TBL] [Abstract][Full Text] [Related]  

  • 47. High resolution replication banding combined with in situ hybridization for the delineation of a subtle chromosome rearrangement.
    Qumsiyeh MB; Wilroy RS; Peeden JN; Tharapel AT
    Am J Med Genet; 1991 Oct; 41(1):99-101. PubMed ID: 1719815
    [TBL] [Abstract][Full Text] [Related]  

  • 48. A severely mentally and motor retarded girl with monosomy 3pter-->p25 and trisomy 8q24-->qter due to a familial reciprocal translocation t(3;8)(p25;q24).
    Balci S; Aypar E; Beksaç MS; Bartsch O
    Genet Couns; 2009; 20(2):125-32. PubMed ID: 19650409
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Trisomy for the distal segment of the short arm of chromosome 17 in a boy with mild mental retardation and some dysmorphic features.
    Mégarbané A; Souraty N; Theophile D; Vekemans M; Samaras L; Ghorayeb Z
    Ann Genet; 1997; 40(1):55-9. PubMed ID: 9150851
    [TBL] [Abstract][Full Text] [Related]  

  • 50. An unusual case of monosomy 18p: minor malformations with speech delay.
    Bora E; Giray O; Ulgenalp A; Ozkan H; Erçal D
    Turk J Pediatr; 2005; 47(2):199-201. PubMed ID: 16052867
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.
    Chen CP; Chern SR; Wang W; Lee CC; Chen WL; Chen LF; Chang TY; Tzen CY
    Prenat Diagn; 2001 May; 21(5):346-50. PubMed ID: 11360273
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Segregation of a paternal insertional translocation results in partial 4q monosomy or 4q trisomy in two siblings.
    Hegmann KM; Spikes AS; Orr-Urtreger A; Shaffer LG
    Am J Med Genet; 1996 Jan; 61(1):10-5. PubMed ID: 8741910
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Pericentric inversion with partial 7(q35-->qter) duplication and 7pter deletion: diagnosis by cytogenetic and fish analysis in a 29-year-old male patient.
    Lukusa T; Van Buggenhout G; Devriendt K; Fryns JP
    Genet Couns; 2002; 13(1):1-10. PubMed ID: 12017231
    [TBL] [Abstract][Full Text] [Related]  

  • 54. A partial trisomy 15q due to 15;17 translocation detected by conventional cytogenetic and FISH techniques.
    Cora T; Acar H; Oran B
    Genet Couns; 2000; 11(1):25-32. PubMed ID: 10756424
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Distal trisomy 10q/partial monosomy 14q: an unusual clinical picture.
    Bregant L; Gersak K; Veble A
    Genet Couns; 2005; 16(1):59-63. PubMed ID: 15844780
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Blepharophimosis and mental retardation (BMR) phenotypes caused by chromosomal rearrangements: description in a boy with partial trisomy 10q and monosomy 4q and review of the literature.
    Bartholdi D; Toelle SP; Steiner B; Boltshauser E; Schinzel A; Riegel M
    Eur J Med Genet; 2008; 51(2):113-23. PubMed ID: 18262484
    [TBL] [Abstract][Full Text] [Related]  

  • 57. A 14-year follow-up of a case detected prenatally of partial trisomy 13q21.32-qter and monosomy 18q22.3-qter as a result of a maternal complex chromosome rearrangement involving chromosomes 6, 13, and 18.
    Quadrelli R; Quadrelli A; Milunsky A; Zou YS; Huang XL; Viera E; Mechoso B; Bellini S; Costabel M; Vaglio A
    Genet Test Mol Biomarkers; 2009 Jun; 13(3):387-93. PubMed ID: 19473082
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Perinatal findings and molecular cytogenetic analysis of trisomy 16q and 22q13.3 deletion.
    Chen CP; Lin SP; Chern SR; Shih SL; Lee CC; Wang W; Liao YW
    Prenat Diagn; 2003 Jun; 23(6):504-8. PubMed ID: 12813767
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Partial monosomy of chromosome 1p36.3: characterization of the critical region and delineation of a syndrome.
    Reish O; Berry SA; Hirsch B
    Am J Med Genet; 1995 Dec; 59(4):467-75. PubMed ID: 8585567
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
    Aglan MS; Kamel AK; Helmy NA
    Genet Couns; 2008; 19(2):199-209. PubMed ID: 18618995
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 40.