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 *

213 related articles for article (PubMed ID: 7252090)

  • 1. [45X/46XY/46XrY mosaic with banding and the Turner phenotype (author's transl)].
    Aubert L; Verdet C; Giraud F; Mattei JF
    J Gynecol Obstet Biol Reprod (Paris); 1981; 10(1):57-60. PubMed ID: 7252090
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Y chromosome structural abnormalities and Turner's syndrome].
    Ravel C; Siffroi JP
    Gynecol Obstet Fertil; 2009 Jun; 37(6):511-8. PubMed ID: 19464936
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Double aneuploidy in three Egyptian patients: Down-Turner and Down-Klinefelter syndromes.
    Zaki MS; Kamel AA; El-Ruby M
    Genet Couns; 2005; 16(4):393-402. PubMed ID: 16440882
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Turner syndrome female with a small ring X chromosome lacking the XIST, an unexpectedly mild phenotype and an atypical association with alopecia universalis.
    Bouayed Abdelmoula N; Portnoï MF; Amouri A; Arladan A; Chakroun M; Saad A; Hchicha M; Turki H; Rebai T
    Ann Genet; 2004; 47(3):305-13. PubMed ID: 15337477
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [A rare structural anomaly of the Y chromosome: Y ring (author's transl)].
    Bühler EM; Tsuchimoto T; Bühler UK; Stalder GR
    Arch Genet (Zur); 1974; 47(1):52-9. PubMed ID: 4469774
    [No Abstract]   [Full Text] [Related]  

  • 7. [Asymmetrical gonadal dysgenesis. Report of a case (author's transl)].
    Chapoy P; Mattei JF; Exbrayat C; Louchet E
    Ann Genet; 1979; 22(3):173-7. PubMed ID: 316676
    [TBL] [Abstract][Full Text] [Related]  

  • 8. H-Y antigen in XO/X,iso(X) mosaic Turner syndrome.
    Meade KW; Wachtel SS; Davis JR; Lightner ES
    Obstet Gynecol; 1981 May; 57(5):594-9. PubMed ID: 7194461
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [45,X/46,X,del(Yq) sex chromosome mosaicism--analysis of the phenotypic expression].
    Werner W; John B; Tuschy U; Knorr B; Herrmann FH
    Zentralbl Gynakol; 1985; 107(5):265-79. PubMed ID: 3993267
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mixed gonadal dysgenesis with 45,X/46,X,idic(Y)/46,XY,idic(Y) karyotype.
    Caglayan AO; Demiryilmaz F; Kendirci M; Ozyazgan I; Akalin H; Bittmann S
    Genet Couns; 2009; 20(2):173-9. PubMed ID: 19650415
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 47,XXX/45,X/46,XX mosaicism in a patient with Turner phenotype and spontaneous puberal development.
    Brambila-Tapia AJ; Rivera H; García-Castillo H; Domínguez-Quezada MG; Dávalos-Rodríguez IP
    Fertil Steril; 2009 Nov; 92(5):1747.e5-7. PubMed ID: 19732877
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Iso-X chromosomes in primary amenorrhoea and Turner's syndrome - presentation by C-banding (author's transl)].
    Zernahle K
    Zentralbl Gynakol; 1980; 102(3):151-60. PubMed ID: 7211028
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mental retardation and Ullrich-Turner syndrome in cases with 45,X/46X,+mar: additional support for the loss of the X-inactivation center hypothesis.
    Cole H; Huang B; Salbert BA; Brown J; Howard-Peebles PN; Black SH; Dorfmann A; Febles OR; Stevens CA; Jackson-Cook C
    Am J Med Genet; 1994 Aug; 52(2):136-45. PubMed ID: 7801998
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Identification of sex chromosome markers using fluorescence in situ hybridization (FISH)].
    González-del-Angel A; Blanco B; del Castillo V; Carnevale A
    Rev Invest Clin; 1995; 47(2):117-25. PubMed ID: 7610280
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 45,X/46,X,dic(Yq) mosaicism and mixed gonadal dysgenesis. Case report and review of the literature.
    Armandares S; Salamanca F; Cos J; Chavarria C
    Ann Genet; 1977 Dec; 20(4):269-72. PubMed ID: 305755
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [A rare case of gonadal dysgenesis with 45, X-46, X ring X mosaic--case report].
    Albert PJ; Gille J; Schmid M
    Geburtshilfe Frauenheilkd; 1986 Jul; 46(7):473-4. PubMed ID: 3758629
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Gonadal mosaicism 45,X/46,X,psu dic(Y)(q11.2) resulting in a Turner phenotype with mixed gonadal dysgenesis.
    Gole LA; Lim J; Crolla JA; Loke KY
    Singapore Med J; 2008 Apr; 49(4):349-51. PubMed ID: 18418530
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Turner syndrome and 45,X/47,XXX mosaicism.
    Akbas E; Mutluhan H; Savasoglu K; Soylemez F; Ozturk I; Yazici G
    Genet Couns; 2009; 20(2):141-6. PubMed ID: 19650411
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [A case of gonadal dysgenesis with 45X-46XXqi mosaicism (autoradiographic study of chromosomes)].
    Guinet P; Laurent C; Nivelon A; Bonhomme J; Mikaelian S
    Rev Lyon Med; 1970 Oct; 19(15):631-8. PubMed ID: 5495951
    [No Abstract]   [Full Text] [Related]  

  • 20. [Identification and characterization of marker chromosome in Turner syndrome].
    Tan YQ; Cheng DH; DI YF; Li LY; Lu GX
    Zhonghua Fu Chan Ke Za Zhi; 2007 Oct; 42(10):679-82. PubMed ID: 18241543
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.