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 *

73 related articles for article (PubMed ID: 1213239)

  • 21. Mixed gonadal dysgenesis with XO-XY mosaicism in multiple tissues. Report of a case.
    Hung W; Verghese KP; Picciano D; Jacobson CB; Chandra R
    Obstet Gynecol; 1970 Sep; 36(3):373-6. PubMed ID: 5465438
    [No Abstract]   [Full Text] [Related]  

  • 22. [Genital malformations in thalidomide-damaged girls (author's transl)].
    Hoffmann W; Grospietsch G; Kuhn W
    Geburtshilfe Frauenheilkd; 1976 Dec; 36(12):1066-70. PubMed ID: 1010296
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Agonadism in a 46,XY patient with CHARGE association.
    Kushnick T; Wiley JE; Palmer SM
    Am J Med Genet; 1992 Jan; 42(1):96-9. PubMed ID: 1308372
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Presence of the Y chromosome in female patients with Turner's syndrome].
    Boczkowski K
    Pol Tyg Lek; 1985 Dec; 40(49):1369-70. PubMed ID: 3831983
    [No Abstract]   [Full Text] [Related]  

  • 25. Scrotal hysterectomy in a male patient with mixed gonadal dysgenesis 46,XY(75%)/45,X(25%).
    Preusser S; Diener PA; l'Allemand-Jander D; Schmid S; Leippold T; Brändle M; Schmid HP
    Urology; 2007 Dec; 70(6):1223.e7-9. PubMed ID: 18158064
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The VCUAM (Vagina Cervix Uterus Adnex-associated Malformation) classification: a new classification for genital malformations.
    Oppelt P; Renner SP; Brucker S; Strissel PL; Strick R; Oppelt PG; Doerr HG; Schott GE; Hucke J; Wallwiener D; Beckmann MW
    Fertil Steril; 2005 Nov; 84(5):1493-7. PubMed ID: 16275249
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Case of male pseudohermaphroditism in cattle. (Bos taurus L.) with a 60 XY karyotype].
    Sysa P; Bernacki Z; Kuńska A
    Pol Arch Weter; 1975; 18(1):143-52. PubMed ID: 1181556
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Gonadal dysgenesis in individuals with apparently normal chromosomal complements: tabulation of cases and compilation of genetic data.
    Simpson JL; Christakos AC; Horwith M; Silverman FS
    Birth Defects Orig Artic Ser; 1971 May; 7(6):215-28. PubMed ID: 5173165
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Mixed gonadal dysgenesis: clinical, cytogenetic, endocrinological, and histopathological findings in 16 patients.
    Méndez JP; Ulloa-Aguirre A; Kofman-Alfaro S; Mutchinick O; Fernández-del-Castillo C; Reyes E; Pérez-Palacios G
    Am J Med Genet; 1993 May; 46(3):263-7. PubMed ID: 8488868
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Asymmetrical gonadal differentiation and gonadoblastoma. Clinical, cytogenetic and histological findings. Case report.
    Coco R; Chemes H; Bergada C
    Acta Endocrinol (Copenh); 1975 Dec; 80(4):753-60. PubMed ID: 1242581
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Complete androgen insensitivity without Wolffian duct development: the AR-A form of the androgen receptor is not sufficient for male genital development.
    Barbaro M; Oscarson M; Almskog I; Hamberg H; Wedell A
    Clin Endocrinol (Oxf); 2007 Jun; 66(6):822-6. PubMed ID: 17408421
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [H-Y antigen and sexual dysgenesis in man].
    Casanova-Bettane M; Fellous M
    C R Seances Soc Biol Fil; 1981; 175(1):8-18. PubMed ID: 6452934
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Analysis of the SRY gene in a girl with 45,X/46,XY genotype.
    Akbas E; Soylemez F; Hallioglu O; Polat S; Turkoz G
    Genet Couns; 2009; 20(3):249-54. PubMed ID: 19852431
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Turner syndrome: II. Associated anomalies, mental performance and psychological problems in 218 patients diagnosed in Leuven in the period 1965-1989.
    Kleczkowska A; Kubien E; Dmoch E; Fryns JP; Van den Berghe H
    Genet Couns; 1990; 1(3-4):241-9. PubMed ID: 2098048
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [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]  

  • 36. Familial occurrence of agonadism and multiple internal malformations in phenotypically normal girls with 46,XY and 46,XX karyotypes, respectively: a new autosomal recessive syndrome.
    Kennerknecht I; Sorgo W; Oberhoffer R; Teller WM; Mattfeldt T; Negri G; Vogel W
    Am J Med Genet; 1993 Dec; 47(8):1166-70. PubMed ID: 8291549
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Testicular regression in a patient with virilized female phenotype.
    Rosenberg C; Mustacchi Z; Braz A; Arnhold IJ; Chu TH; Carnevale J; Frota-Pessoa O
    Am J Med Genet; 1984 Sep; 19(1):183-8. PubMed ID: 6437223
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Sex chromosome mosaicism of X/XY or X/XY/XYY.
    Wilson MG; Ebbin AJ; Shinno NW; Towner JW
    Birth Defects Orig Artic Ser; 1975; 11(5):255-66. PubMed ID: 1218222
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Phenotypic spectrum of 45,X/46,XY individuals.
    Rosenberg C; Frota-Pessoa O; Vianna-Morgante AM; Chu TH
    Am J Med Genet; 1987 Jul; 27(3):553-9. PubMed ID: 3631129
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.