These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

192 related articles for article (PubMed ID: 6660249)

  • 1. Ring chromosome 6: variability in phenotypic expression.
    Peeden JN; Scarbrough P; Taysi K; Wilroy RS; Finley S; Luthardt F; Martens P; Howard-Peebles PN
    Am J Med Genet; 1983 Dec; 16(4):563-73. PubMed ID: 6660249
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The syndrome of ring chromosome 12.
    Scribanu N; McCullars EB; Baumiller RC; Colon AR
    Am J Med Genet; 1980; 5(2):165-70. PubMed ID: 7395909
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes.
    Callen DF; Eyre H; Yip MY; Freemantle J; Haan EA
    Am J Med Genet; 1992 Jul; 43(4):709-15. PubMed ID: 1377870
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Transmission of an 18 ring chromosome in two generations in subjects of normal phenotype].
    Faugeras C; Barthe D
    J Genet Hum; 1986 Aug; 34(3-4):313-20. PubMed ID: 3760834
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Small accessory chromosomes (SAC) and their genotype--phenotype correlation.
    Fryns JP; Kleczkowska A; Van den Berghe H
    J Genet Hum; 1982 Oct; 30(3):215-32. PubMed ID: 7153768
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Observation of 7 cases of rare autosomal pathology. Trisomy 9p; monosomy 18q; ring 21; trisomy 6p; trisomy 2q 1-21 translocation].
    Fioretti G; Pagano L; Renda S; Festa B; Rinaldi A; Celona A; Casullo C; Stabile M; Cavaliere ML; Ventruto V
    Minerva Pediatr; 1980 Jun; 32(12):807-14. PubMed ID: 7464734
    [No Abstract]   [Full Text] [Related]  

  • 7. Brief clinical report: ring-11 chromosome: phenotype-karyotype correlation with deletions of 11q.
    Cousineau AJ; Higgins JV; Scott-Emuakpor AB; Mody G
    Am J Med Genet; 1983 Jan; 14(1):29-35. PubMed ID: 6829609
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Ring chromosome 9: identification of a new case by G- and C-banding.
    Dipierri JE; Matayoshi T
    Ann Genet; 1982; 25(4):243-5. PubMed ID: 6985015
    [No Abstract]   [Full Text] [Related]  

  • 9. [Chromosome analysis and phenotype location analysis on a patient with the karyotype of 45, XX, -13/46, XX, r(13)/46, XX, r(13;13)/47, XX, 2r(13)(p13q32.3)].
    Liang DS; Wu LQ; Long ZG; Pan Q; Dai HP; Xia JH
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Aug; 21(4):392-4. PubMed ID: 15300643
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Five cases of supernumerary small ring chromosomes 1: heterogeneity and genotype-phenotype correlation.
    Bernardini L; Capalbo A; D'Avanzo MG; Torrente I; Grammatico P; Dell'Edera D; Cavalcanti DP; Novelli A; Dallapiccola B
    Eur J Med Genet; 2007; 50(2):94-102. PubMed ID: 17236832
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Case report of mosaic partial tetrasomy 9 mimicking Klinefelter syndrome.
    Peters J; Pehl C; Miller K; Sandlin CJ
    Birth Defects Orig Artic Ser; 1982; 18(3B):287-93. PubMed ID: 7139111
    [No Abstract]   [Full Text] [Related]  

  • 12. Non-mosaic trisomy 16 in a third-trimester fetus.
    Yancey MK; Hardin EL; Pacheco C; Kuslich CD; Donlon TA
    Obstet Gynecol; 1996 May; 87(5 Pt 2):856-60. PubMed ID: 8677115
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Ring chromosome 21 in a normal female.
    Kleczkowska A; Fryns JP
    Ann Genet; 1984; 27(2):126-8. PubMed ID: 6331791
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Analysis of banding patterns in a case of ring chromosome 21.
    Richer CL; Fitch N; Sitahal S; Murer-Orlando M; Jean P
    Am J Med Genet; 1981; 10(4):323-31. PubMed ID: 7332027
    [No Abstract]   [Full Text] [Related]  

  • 15. Identification of marker chromosomes in thirteen patients using FISH probing.
    Daniel A; Malafiej P; Preece K; Chia N; Nelson J; Smith M
    Am J Med Genet; 1994 Oct; 53(1):8-18. PubMed ID: 7802042
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Ring chromosome 14. A distinct clinical entity.
    Fryns JP; Kubien E; Kleczkowska A; Nawrocka-Kanska B; Van den Berghe H
    J Genet Hum; 1983 Dec; 31 Suppl 5():367-75. PubMed ID: 6674412
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Phenotype/karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases.
    Hsu LY
    Am J Med Genet; 1994 Nov; 53(2):108-40. PubMed ID: 7856637
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Duplication of euchromatin without phenotypic effects: a variant of chromosome 16.
    Bryke CR; Breg WR; Potluri VR; Yang-Feng TL
    Am J Med Genet; 1990 May; 36(1):43-4. PubMed ID: 2333906
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [A new case of ring chromosome 9].
    Portnoi MF; van den Akker J; Le Porrier N; Joye N; Youssef S; Taillemite JL
    Ann Genet; 1982; 25(3):164-7. PubMed ID: 6982668
    [No Abstract]   [Full Text] [Related]  

  • 20. Phenotype associated with ring 10 chromosome: report of patient and review of literature.
    Michels VV; Driscoll DJ; Ledbetter DH; Riccardi VM
    Am J Med Genet; 1981; 9(3):231-7. PubMed ID: 7025632
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.