BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

247 related articles for article (PubMed ID: 8230159)

  • 1. High resolution mapping of interstitial long arm deletions of chromosome 16: relationship to phenotype.
    Callen DF; Eyre H; Lane S; Shen Y; Hansmann I; Spinner N; Zackai E; McDonald-McGinn D; Schuffenhauer S; Wauters J
    J Med Genet; 1993 Oct; 30(10):828-32. PubMed ID: 8230159
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular analysis redefines three human chromosome 14 deletions.
    Wintle RF; Costa T; Haslam RH; Teshima IE; Cox DW
    Hum Genet; 1995 May; 95(5):495-500. PubMed ID: 7759068
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Interstitial deletion of the short arm of chromosome 4.
    Ray M; Evans J; Rockman-Greenberg C; Wickstrom D
    J Med Genet; 1984 Jun; 21(3):223-5. PubMed ID: 6748021
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A unique de novo interstitial deletion del(17)(q21.3q23) in a phenotypically abnormal infant.
    Park JP; Moeschler JB; Berg SZ; Bauer RM; Wurster-Hill DH
    Clin Genet; 1992 Jan; 41(1):54-6. PubMed ID: 1633649
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Terminal deletion of the long arm of chromosome 4 in a mother and two sons.
    Descartes M; Keppler-Noreuil K; Knops J; Longshore JW; Finley WH; Carroll AJ
    Clin Genet; 1996 Dec; 50(6):538-40. PubMed ID: 9147894
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 16q21 is critical for 16q deletion syndrome.
    Naritomi K; Shiroma N; Izumikawa Y; Sameshima K; Ohdo S; Hirayama K
    Clin Genet; 1988 May; 33(5):372-5. PubMed ID: 3378367
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular analysis of the 18q- syndrome--and correlation with phenotype.
    Kline AD; White ME; Wapner R; Rojas K; Biesecker LG; Kamholz J; Zackai EH; Muenke M; Scott CI; Overhauser J
    Am J Hum Genet; 1993 May; 52(5):895-906. PubMed ID: 8488839
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genotype-phenotype mapping of chromosome 18q deletions by high-resolution array CGH: an update of the phenotypic map.
    Feenstra I; Vissers LE; Orsel M; van Kessel AG; Brunner HG; Veltman JA; van Ravenswaaij-Arts CM
    Am J Med Genet A; 2007 Aug; 143A(16):1858-67. PubMed ID: 17632778
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Interstitial deletion and ring chromosome derived from 16q.
    Krauss CM; Caldwell D; Atkins L
    J Med Genet; 1987 May; 24(5):308-12. PubMed ID: 3585948
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Smith-Magenis syndrome: a new contiguous gene syndrome. Report of three new cases.
    Moncla A; Livet MO; Auger M; Mattei JF; Mattei MG; Giraud F
    J Med Genet; 1991 Sep; 28(9):627-32. PubMed ID: 1956064
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Interstitial deletion of the long arm of chromosome 5 in a deformed boy: 46,XY,del(5)(q13q15).
    Stoll C; Levy J; Roth MP
    J Med Genet; 1980 Dec; 17(6):486-7. PubMed ID: 7205434
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Multiple critical smallest region of overlap in monosomy 16Q syndrome?
    Doco-Fenzy M; Elchardus JF; Brami G; Digeon B; Gruson N; Adnet JJ
    Genet Couns; 1994; 5(1):39-44. PubMed ID: 8031534
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Williams syndrome and chromosome 18.
    Menko FH; Stouthart PJ
    J Med Genet; 1992 Sep; 29(9):679-80. PubMed ID: 1404306
    [No Abstract]   [Full Text] [Related]  

  • 14. A case of partial monosomy 21q22.2 associated with Rieger's syndrome.
    Nielsen F; Trånebjaerg L
    J Med Genet; 1984 Jun; 21(3):218-21. PubMed ID: 6431108
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A detailed investigation of two cases exhibiting characteristics of the 6p deletion syndrome.
    Davies AF; Olavesen MG; Stephens RJ; Davidson R; Delneste D; Van Regemorter N; Vamos E; Flinter F; Abusaad I; Ragoussis J
    Hum Genet; 1996 Oct; 98(4):454-9. PubMed ID: 8792822
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Distal monosomy of the long arm of chromosome 6 (6q25----6qter) inherited by maternal translocation t(6q;17q).
    Oliveira-Duarte MH; Martelli-Soares LR; Sarquis-Cintra T; Machado ML; Lison MP
    Ann Genet; 1990; 33(1):56-9. PubMed ID: 2195984
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Determination of the breakpoints and the parental origin of a ring 22 chromosome: an analysis by high-resolution banding technique, quinacrine and silver stainings.
    Naritomi K; Hirayama K
    Jinrui Idengaku Zasshi; 1988 Mar; 33(1):67-73. PubMed ID: 2455825
    [No Abstract]   [Full Text] [Related]  

  • 18. A familial interstitial deletion of the long arm of chromosome 21.
    Roland B; Cox DM; Hoar DI; Fowlow SB; Robertson AS
    Clin Genet; 1990 Jun; 37(6):423-8. PubMed ID: 2383928
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Partial monosomy of long arm of chromosome 4 due to interstitial deletion.
    McDermott A; Cain R; Howell R
    Hum Genet; 1980; 53(3):305-7. PubMed ID: 7372333
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A refined physical map of the long arm of human chromosome 16.
    Chen LZ; Harris PC; Apostolou S; Baker E; Holman K; Lane SA; Nancarrow JK; Whitmore SA; Stallings RL; Hildebrand CE
    Genomics; 1991 Jun; 10(2):308-12. PubMed ID: 2071140
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.