BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

115 related articles for article (PubMed ID: 699362)

  • 1. Partial trisomy 15 and temporal lobe syndrome in a retarded girl without gross malformations.
    Hongell K; Iivanainen M
    Clin Genet; 1978 Oct; 14(4):229-34. PubMed ID: 699362
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Extra dicentric 15 pter leads to q21/22 chromosomes in five unrelated patients with a distinct syndrome of progressive psychomotor retardation, seizures, hyper-reactivity and dermatoglyphic abnormalities.
    Zannotti M; Preto A; Giovanardi PR; Dallapiccola B
    J Ment Defic Res; 1980 Dec; 24 Pt 4():235-42. PubMed ID: 7218339
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Parental origin of the extra chromosome in the cat eye syndrome: evidence from heteromorphism and in situ hybridization analysis.
    Magenis RE; Sheehy RR; Brown MG; McDermid HE; White BN; Zonana J; Weleber R
    Am J Med Genet; 1988 Jan; 29(1):9-19. PubMed ID: 3344779
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A case of extra small acrocentric bisatellited chromosome in a non mongoloid child.
    Furbetta M; Rosi G; Biagioni M; Cossu P; Cao A
    Humangenetik; 1975 Sep; 30(3):259-63. PubMed ID: 1184008
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Trisomy 13 in a 4-year-old child.
    Fernández-Novoa C; Hevia A; Martínez JJ; San Martín V; Galera H
    Hum Genet; 1980; 53(3):297-8. PubMed ID: 7372331
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Two children with deletion of the long arm of chromosome 4 with breakpoint at band q33.
    Tomkins DJ; Hunter AG; Uchida IA; Roberts MH
    Clin Genet; 1982 Dec; 22(6):348-55. PubMed ID: 7160106
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).
    Schinzel A; Hayashi K; Schmid W
    Humangenetik; 1975 Dec; 30(4):307-16. PubMed ID: 1218860
    [TBL] [Abstract][Full Text] [Related]  

  • 8. An extra small metacentric chromosome identified as a deleted chromosome no. 17.
    Palutke W; Chen H; Woolley P; Espiritu C; Vogel HL; Gohle N; Tyrkus M
    Clin Genet; 1976 May; 9(5):454-58. PubMed ID: 1269167
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Partial trisomy 13 plus partial trisomy 4q due to unusual segregation of translocation chromosomes.
    Fonatsch C; Flatz SD; Weitzel E
    Clin Genet; 1979 Feb; 15(2):176-82. PubMed ID: 761418
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX, - 13, + t(13;13)(p11;q11)/46,XX,del(13)(p11).
    Fryns JP; Casaer P; Van den Berghe H
    Hum Genet; 1979 Jan; 46(2):237-41. PubMed ID: 422207
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Partial trisomy 14q.
    Lopez Pajares I; Delicado A; Cobos PV; Lledo G; Peralta A
    Hum Genet; 1979 Jan; 46(2):243-7. PubMed ID: 422208
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Analysis of banding patterns and mosaic configurations in a case of ring chromosome 15.
    Schmid M; Henrichs I; Nestler H; Knörr-Gärtner H; Teller WM; Krone W
    Hum Genet; 1978 Apr; 41(3):289-99. PubMed ID: 649157
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Complete trisomy 22.
    Shokeir MH
    Clin Genet; 1978 Sep; 14(3):139-46. PubMed ID: 568044
    [TBL] [Abstract][Full Text] [Related]  

  • 14. De novo partial trisomy 15q (proximal type).
    Herweijer TJ; Oorthuys JW; Leschot NJ
    J Med Genet; 1988 Apr; 25(4):260-2. PubMed ID: 2966860
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Partial trisomy of chromosome no. 1 in two adult brothers due to maternal translocation (1q--;6p+).
    Taysi K; Sekhon GS
    Hum Genet; 1978 Nov; 44(3):277-85. PubMed ID: 730168
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Partial trisomy 12q24.31----qter.
    Tajara EH; Varella-Garcia M; Gusson AC
    J Med Genet; 1985 Feb; 22(1):73-6. PubMed ID: 3981585
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Partial trisomy 11q as the result of sporadic translocation.
    Lurie IW; Lazjuk GI; Usova YI; Gurevich DB
    Hum Genet; 1979 Sep; 51(1):63-6. PubMed ID: 500093
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Partial trisomy of the short arm of chromosome 7 due to a familial translocation rcp(7;14)(p11;p11).
    Carnevale A; Frías S; del Castillo V
    Clin Genet; 1978 Oct; 14(4):202-6. PubMed ID: 699358
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Partial trisomy 15q due to maternal translocation t(7;15)(q35;14)].
    Castel Y; Rivière D; Boycly JY; Toudic L
    Ann Genet; 1976 Mar; 19(1):15-9. PubMed ID: 1084116
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Trisomy 17p due to a t(8;17) (p23;p11.2)pat translocation. Case report and review of the literature.
    Schrander-Stumpel C; Schrander J; Fryns JP; Hamers G
    Clin Genet; 1990 Feb; 37(2):148-52. PubMed ID: 2178819
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.