BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

181 related articles for article (PubMed ID: 7154050)

  • 1. Interstitial deletion of the long arm of chromosome 5: 46,XX,del(5)(q13q22).
    Ohdo S; Madokoro H; Hayakawa K
    J Med Genet; 1982 Dec; 19(6):479. PubMed ID: 7154050
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. Two cases of interstitial deletion of the long arm of chromosome 1: del(1)(q21----q25) and del(1)(q41----q43).
    Beemer FA; Klep-de Pater JM; Sepers GJ; Janssen B
    Clin Genet; 1985 May; 27(5):515-9. PubMed ID: 4006278
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Interstitial deletion of the long arm of chromosome 4 in a patient with mental retardation and abnormal phenotype.
    del Valle Torrado M; Labarta JD; Migliorini AM
    J Med Genet; 1982 Dec; 19(6):477. PubMed ID: 6185682
    [No Abstract]   [Full Text] [Related]  

  • 7. Genetic and clinical studies in 13 patients with the Wolf-Hirschhorn syndrome [del(4p)].
    Wilson MG; Towner JW; Coffin GS; Ebbin AJ; Siris E; Brager P
    Hum Genet; 1981; 59(4):297-307. PubMed ID: 6949855
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 4p- syndrome in a girl with translocation t(1;4)(q11;p16)mat.
    Stoll C; Pennerath A; Lausecker C
    Hum Genet; 1981; 56(3):413-5. PubMed ID: 7239524
    [No Abstract]   [Full Text] [Related]  

  • 9. Complex MCA/MR syndrome associated with interstitial deletion of the long arm of chromosome 6, del(6)(q25.1-->q27).
    Vermeesch JR; Fryns JP
    Am J Med Genet A; 2003 Jul; 120A(2):299-300. PubMed ID: 12833421
    [No Abstract]   [Full Text] [Related]  

  • 10. The 11q- syndrome with mosaic partial deletion of 11q.
    Ishida Y; Watanabe N; Ishihara Y; Matsuda H
    Acta Paediatr Jpn; 1992 Dec; 34(6):592-6. PubMed ID: 1285504
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Simultaneous de novo interstitial deletion of 16q21 and intercalary duplication of 19q in a retarded infant with minor dysmorphic features.
    Trautmann U; Pfeiffer RA; Seufert-Satomi U; Tietze HU
    J Med Genet; 1993 Apr; 30(4):330-1. PubMed ID: 8487285
    [TBL] [Abstract][Full Text] [Related]  

  • 12. De novo interstitial deletion of the long arm of chromosome 7:46,XY,del(7)(q23;q32).
    Martin-Pont B; Pilczer C; Dandine M; Tamboise A
    Ann Genet; 1985; 28(4):251-3. PubMed ID: 3879441
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A case of de novo interstitial deletion 3q.
    Okada N; Hasegawa T; Osawa M; Fukuyama Y
    J Med Genet; 1987 May; 24(5):305-8. PubMed ID: 3585947
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Developmental abnormalities associated with long arm deletion of chromosome No. 6.
    Bartoshesky L; Lewis MB; Pashayan HM
    Clin Genet; 1978 Jan; 13(1):68-71. PubMed ID: 624189
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Syndromes associated with deletion of the long arm of chromosome 18[del(18q)].
    Wilson MG; Towner JW; Forsman I; Siris E
    Am J Med Genet; 1979; 3(2):155-74. PubMed ID: 474629
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Three cases of 16q duplication.
    Maher ER; Willatt L; Cuthbert G; Chapman C; Hodgson SV
    J Med Genet; 1991 Nov; 28(11):801-2. PubMed ID: 1820771
    [No Abstract]   [Full Text] [Related]  

  • 17. Interstitial deletion of band q12 of chromosome 5.
    Dudin G; Alexander D; Talj F; Deeb M; Musallam S; Der Kaloustian VM
    Clin Genet; 1984 May; 25(5):455-8. PubMed ID: 6723107
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Another patient with an interstitial deletion of chromosome 9: case report and a review of six cases with del(9)(q22q32).
    Kroes HY; Tuerlings JH; Hordijk R; Folkers NR; ten Kate LP
    J Med Genet; 1994 Feb; 31(2):156-8. PubMed ID: 8182726
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Deletion of chromosome 2 (p11-p13): case report and review.
    Prasher VP; Krishnan VH; Clarke DJ; Maliszewska CT; Corbett JA
    J Med Genet; 1993 Jul; 30(7):604-6. PubMed ID: 8411037
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Terminal deletion(4)(q33) in a male infant.
    Stamberg J; Jabs EW; Elias E
    Clin Genet; 1982 Feb; 21(2):125-9. PubMed ID: 7083613
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.