BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

155 related articles for article (PubMed ID: 7211840)

  • 1. Study of two cases of ring 13 chromosome using high-resolution banding.
    Jones IM; Palmer CG; Weaver DD; Hodes ME
    Am J Hum Genet; 1981 Mar; 33(2):252-61. PubMed ID: 7211840
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A case of mosaic trisomy 14 due to an isochromosome, i(14q).
    Ozawa N; Xu ZD; Soh K; Takabayashi T; Sato S; Yajima A; Suzuki M; Ikeuchi T; Tonomura A
    Jinrui Idengaku Zasshi; 1984 Mar; 29(1):69-76. PubMed ID: 6748330
    [No Abstract]   [Full Text] [Related]  

  • 3. Ring chromosome 15: phenotype, Ag-NOR analysis, secondary aneuploidy, and associated chromosome instability.
    Ledbetter DH; Riccardi VM; Au WW; Wilson DP; Holmquist GP
    Cytogenet Cell Genet; 1980; 27(2-3):111-22. PubMed ID: 6156798
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. A complex mosaic with tdic(13;18) (p11;p11), +13p-, +18p-, r(13) etc. in a male infant. I. Centromere inactivation and dissociation of dicentric chromosome.
    Uehara M; Kida M
    Jinrui Idengaku Zasshi; 1986 Mar; 31(1):27-35. PubMed ID: 3735756
    [No Abstract]   [Full Text] [Related]  

  • 6. 13q-/r(13) mosaicism.
    Niikawa N; Tamura T; Tomiyasu F; Kajii T
    J Med Genet; 1980 Aug; 17(4):316-9. PubMed ID: 7205909
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Malformative syndrome with ring chromosome 13.
    Fryns JP; Deoover J; Van den Berghe H
    Humangenetik; 1974; 24(3):235-40. PubMed ID: 4140834
    [No Abstract]   [Full Text] [Related]  

  • 8. Ring chromosome 14: a distinct clinical entity.
    Schmidt R; Eviatar L; Nitowsky HM; Wong M; Miranda S
    J Med Genet; 1981 Aug; 18(4):304-7. PubMed ID: 7277427
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 18q- and 18q+ mosaicism in a mentally retarded boy.
    Ausems MG; Bhola SL; Post-Blok CA; Hennekam RC; de France HF
    Am J Med Genet; 1994 Nov; 53(3):296-9. PubMed ID: 7856666
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Partial trisomy 15 in a male with severe psychomotor retardation (48, XY, + 15q -, + mar(15)).
    Voss R; Lerer I; Maftzir G; Sheinis M; Cohen MM
    Am J Med Genet; 1982 Jun; 12(2):131-9. PubMed ID: 7102721
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Tandem duplication (5q13 to 22) in a mentally deficient girl.
    Kessel E; Pfeiffer RA
    Hum Genet; 1979 Nov; 52(2):217-20. PubMed ID: 511177
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Some clinical and cytogenetic observations on a ring chromosome 13 (p11 q34).
    Hernandez A; Garcia-Cruz D; Plascencia L; Nazara Z; Rivera H; Sanchez-Corona J; Cantu JM
    Ann Genet; 1979; 22(4):221-4. PubMed ID: 317785
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A complex mosaic with tdic(13;18) (p11;p11), +13p-, +18p-, r(13) etc. in a male infant. II. Increased dissociation of dicentric chromosome by mitomycin C.
    Uehara M; Kida M
    Jinrui Idengaku Zasshi; 1986 Mar; 31(1):37-43. PubMed ID: 3090320
    [No Abstract]   [Full Text] [Related]  

  • 14. Ring chromosome 14 in a mentally retarded girl.
    Iselius L; Ritzén M; Bui TH; Olsson K; Eklöf O
    Acta Paediatr Scand; 1980 Nov; 69(6):803-6. PubMed ID: 7211367
    [TBL] [Abstract][Full Text] [Related]  

  • 15. High resolution pattern of an inverted duplication (15).
    Hoo JJ
    Clin Genet; 1986 Mar; 29(3):241-5. PubMed ID: 3457663
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 13S+. Giant satellites or de novo rearrangement?
    Imaizumi K; Kajii T; Niikawa N
    Hum Genet; 1981; 59(3):266-8. PubMed ID: 7327588
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Uniparental isodisomy due to duplication of chromosome 21 occurring in somatic cells monosomic for chromosome 21.
    Petersen MB; Bartsch O; Adelsberger PA; Mikkelsen M; Schwinger E; Antonarakis SE
    Genomics; 1992 Jun; 13(2):269-74. PubMed ID: 1351865
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Ring chromosome 13 and multiple malformations (author's transl)].
    Antich J; Plaza J; Geán E
    An Esp Pediatr; 1981 Nov; 15(5):469-73. PubMed ID: 7332149
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cytogenetic and clinical studies in five cases of inv dup(15).
    Wisniewski L; Hassold T; Heffelfinger J; Higgins JV
    Hum Genet; 1979 Sep; 50(3):259-70. PubMed ID: 489010
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.