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 *

163 related articles for article (PubMed ID: 7154047)

  • 1. 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]  

  • 2. [Turner's syndrome--correlation between karyotype and phenotype].
    Lacka K
    Endokrynol Pol; 2005; 56(6):986-93. PubMed ID: 16821224
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cytological findings of 10 cases with i(Xq) and one with dic(X)(qter leads to cen leads to p22::p11 leads to qter).
    Fujita H; Tanigawa Y; Yoshida Y; Okada Y
    Hum Genet; 1977 Nov; 39(2):147-55. PubMed ID: 598825
    [No Abstract]   [Full Text] [Related]  

  • 4. An isodicentric X chromosome with short arm fusion in a woman without somatic features of Turner's syndrome.
    Barnes IC; Curtis DJ; Duncan SL
    J Med Genet; 1987 Jul; 24(7):428-31. PubMed ID: 3612719
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Partial X chromosome trisomy with functional disomy of Xp due to failure of X inactivation.
    Gustashaw KM; Zurcher V; Dickerman LH; Stallard R; Willard HF
    Am J Med Genet; 1994 Oct; 53(1):39-45. PubMed ID: 7802034
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 46,X,i(Xq)/47,XX,+13 mosaicism.
    Igarashi M; Tsukahara M; Sugio Y; Katayama K; Kajii T
    Ann Genet; 1985; 28(4):241-4. PubMed ID: 3879438
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Double trisomy 48,XXX,+ 18 in a newborn.
    Rosenfeld W; Verma RS; Jhaveri RC; Salazar D; Dosik H
    Am J Med Genet; 1981; 8(1):67-71. PubMed ID: 7246607
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Twin pregnancy in woman with 45,X/47,XXX karyotype.
    Kivinen S; Herva R
    Obstet Gynecol; 1980 Sep; 56(3):401-2. PubMed ID: 7422184
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Karyotype/phenotype correlation in females with short stature.
    Temtamy SA; Ghali I; Salam MA; Hussein FH; Ezz EH; Salah N
    Clin Genet; 1992 Mar; 41(3):147-51. PubMed ID: 1563089
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A finding in genetic polymorphism analysis study: A case of non-mosaic 47, XXX without manifestations.
    Yang X; Ye Z; Zhang X; Wang H; Liu C
    Leg Med (Tokyo); 2017 Jul; 27():38-42. PubMed ID: 28697408
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Translocation(X;Y)(p22.33;p11.2) in XX males: etiology of male phenotype.
    Magenis RE; Webb MJ; McKean RS; Tomar D; Allen LJ; Kammer H; Van Dyke DL; Lovrien E
    Hum Genet; 1982; 62(3):271-6. PubMed ID: 6892019
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cytogenetic and clinical studies in gonadal dysgenesis with 46,X,Xt(qter leads to p221::p223 leads to qter) karyotype: review and phenotype/karyotype correlations.
    Ferraro M; De Capoa A; Mostacci C; Pelliccia F; Zulli P; Baldini MA; Di Nisio Q
    J Med Genet; 1980 Dec; 17(6):457-63. PubMed ID: 7205428
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Brief clinical report: del(X) (q26) in a phenotypically normal woman and her daughter who also has trisomy 21.
    Taysi K
    Am J Med Genet; 1983 Feb; 14(2):367-72. PubMed ID: 6188379
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Karyotype-phenotype correlation in females with X chromosome abnormalities.
    Kosmaidou-Aravidou Z
    Ann N Y Acad Sci; 1997 Jun; 816():373-7. PubMed ID: 9238290
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular cytogenetic analysis of a duplication Xp in a female with an abnormal phenotype and random X inactivation.
    Portnoï MF; Bouayed-Abdelmoula N; Mirc M; Zemni R; Castaing H; Stephann J; Ardalan A; Vialard F; Nouchy M; Daoud P; Chelly J; Taillemite JL
    Clin Genet; 2000 Aug; 58(2):116-22. PubMed ID: 11005144
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Tall stature, gonadal dysgenesis, and stigmata of Turner's syndrome caused by a structurally altered X chromosome.
    Binder G; Eggermann T; Enders H; Ranke MB; Dufke A
    J Pediatr; 2001 Feb; 138(2):285-7. PubMed ID: 11174634
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Assessment of X bends in patients with atypical X chromosome phenotypes.
    Munn CA; Wenger SL; Steele MW
    Ann Genet; 1991; 34(2):120-4. PubMed ID: 1746882
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Identification of Y chromosome material in an XX male by means of fluorescent in situ hybridization].
    Brandt CA; Hindkjaer J; Strømkjaer H; Christensen MF; Kølvraa S
    Ugeskr Laeger; 1992 Nov; 154(47):3321-4. PubMed ID: 1462437
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.