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 *

136 related articles for article (PubMed ID: 1219118)

  • 1. Differences in human X isochromosomes.
    Priest JH; Blackston RD; Au KS; Ray SL
    J Med Genet; 1975 Dec; 12(4):378-89. PubMed ID: 1219118
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Further dicentric X isochromosomes and deletions, and a new structure i(X)(pter to q2102 to pter).
    Daniel A; Saville T; Southall DB
    J Med Genet; 1979 Aug; 16(4):278-84. PubMed ID: 490580
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Familial occurrence of isodicentric X chromosomes with different breakpoints.
    Midro AT; Kulikowski M; Sawicka A; Panasiuk B; Korsak E
    Clin Genet; 1988 Sep; 34(3):153-60. PubMed ID: 3180502
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Two dicentric Y isochromosomes, one without and the Yqh heterochromatic segment: review of the Y isochromosomes.
    Daniel A; Lyons N; Casey JH; Gras L
    Hum Genet; 1980; 54(1):31-9. PubMed ID: 7190126
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Pregnancy in a patient with 47,XX,i(Xq) karyotype.
    King CR; Schimke RN
    J Med Genet; 1982 Dec; 19(6):467-9. PubMed ID: 7154047
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formation.
    Wolff DJ; Miller AP; Van Dyke DL; Schwartz S; Willard HF
    Am J Hum Genet; 1996 Jan; 58(1):154-60. PubMed ID: 8554051
    [TBL] [Abstract][Full Text] [Related]  

  • 7. DNA replication and inactivation patterns in structural abnormality of sex chromosomes. I.X-A translocations, rings, fragments, isochromosomes, and pseudo-isodicentrics.
    Camargo M; Cervenka J
    Hum Genet; 1984; 67(1):37-47. PubMed ID: 6745924
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Variant Turner features in a female with X-isochromosome [46,X, i(Xq)]: is it a distinct clinical entity?
    Verma RS; Vedbrat S; Khan F; Dosik H
    Ann Genet; 1981; 24(1):57-60. PubMed ID: 6971622
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Segregation of an X ring chromosome in two generations.
    Dallapiccola B; Bruni L; Boscherini B; Pasquino AM; Chessa L; Vignetti P
    J Med Genet; 1980 Aug; 17(4):306-8. PubMed ID: 7205906
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Homodicentric chromosomes: a distinctive type of dicentric chromosome.
    Ward BE; Bradley CM; Cooper JB; Robinson A
    J Med Genet; 1981 Feb; 18(1):54-8. PubMed ID: 7252999
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Dicentric X isochromosomes in man.
    Howell RT; Roberts SH; Beard RJ
    J Med Genet; 1976 Dec; 13(6):496-500. PubMed ID: 1018308
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Isodicentric X chromosome and mosaicism: report on two cases of 45,X/46,X,idic(Xq)/47,X,idic(Xq),idic(Xq) and review of the literature.
    Melaragno MI; Fakih LM; Cernach MC; Maccagnan P
    Am J Med Genet; 1993 Sep; 47(3):357-9. PubMed ID: 8135281
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Turner syndrome isochromosome karyotype correlates with decreased dental crown width.
    Rizell S; Barrenäs ML; Andlin-Sobocki A; Stecksén-Blicks C; Kjellberg H
    Eur J Orthod; 2012 Apr; 34(2):213-8. PubMed ID: 21303812
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Inherited X-chromosome inverted tandem duplication in a male traced to a grandparental mitotic error.
    Schwartz S; Schwartz MF; Panny SR; Peterson CJ; Waters E; Cohen MM
    Am J Hum Genet; 1986 May; 38(5):741-50. PubMed ID: 3459356
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A familial Xp+ chromosome detected during fetal karyotyping, which is associated with short stature in four generations of a Turkish family.
    Karaman B; Wollnik B; Ermiş H; Yüksel-Apak M; Başaran S
    Prenat Diagn; 2003 Apr; 23(4):336-9. PubMed ID: 12673642
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Opposite deletions/duplications of the X chromosome: two novel reciprocal rearrangements.
    Giglio S; Pirola B; Arrigo G; Dagrada P; Bardoni B; Bernardi F; Russo G; Argentiero L; Forabosco A; Carrozzo R; Zuffardi O
    Eur J Hum Genet; 2000 Jan; 8(1):63-70. PubMed ID: 10713889
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Formation of supernumerary euchromatic short arm isochromosomes: parent and cell stage of origin in new cases and review of the literature.
    Eggermann T; Schubert R; Engels H; Apacik C; Stengel-Rutkowski S; Haefliger C; Emiliani V; Ricagni C; Schwanitz G
    Ann Genet; 1999; 42(2):75-80. PubMed ID: 10434120
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Isochromosomes 12p and 9p: parental origin and possible mechanisms of formation.
    Dutly F; Balmer D; Baumer A; Binkert F; Schinzel A
    Eur J Hum Genet; 1998; 6(2):140-4. PubMed ID: 9781058
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Endocrine, cytogenetic and psychometric features of patients with X-isochromosome 46, X, i(Xq) Turner's syndrome: a preliminary study in nine patients.
    Zinman B; Kabiawu SI; Moross T; Berg J; Lupmanis A; Markovic V; Gardner HA
    Clin Invest Med; 1984; 7(3):135-41. PubMed ID: 6518681
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Replication patterns of human X isochromosomes by high-resolution banding.
    Artifoni L; Baccichetti C; Piovan E; Anglani F; Lenzini E; Goppion G; Tenconi R
    Cytogenet Cell Genet; 1983; 36(4):649-51. PubMed ID: 6661931
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.