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 *

113 related articles for article (PubMed ID: 6070891)

  • 1. Male pseudohermaphroditism and pure gonadal dysgenesis in sisters.
    Barr ML; Carr DH; Plunkett ER; Soltan HC; Wiens RG
    Am J Obstet Gynecol; 1967 Dec; 99(8):1047-55. PubMed ID: 6070891
    [No Abstract]   [Full Text] [Related]  

  • 2. Familial XY gonadal dysgenesis.
    Chemke J; Carmichael R; Stewart JM; Geer RH; Robinson A
    J Med Genet; 1970 Jun; 7(2):105-11. PubMed ID: 5519594
    [No Abstract]   [Full Text] [Related]  

  • 3. [Mixed gonadal dysgenesis: A report of seven cases (author's transl)].
    Takayasu H; Fukutani K; Ishida H; Isurugi K; Kinoshita K
    Nihon Hinyokika Gakkai Zasshi; 1977 Nov; 68(11):1072-83. PubMed ID: 604600
    [No Abstract]   [Full Text] [Related]  

  • 4. Presence of Turner stigmata in a case of dysgenetic male pseudohermaphroditism with 45,X/46,X+mar karyotype.
    Hashimoto H; Maruyama H; Koshida R; Okuda N; Murayama K; Katsumi T; Watanabe K; Sato T
    Arch Dis Child; 1997 Mar; 76(3):268-71. PubMed ID: 9135271
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Sex chromosome and chromatin examination in gynecology.
    Ge QS; Huang LY; Tang MY; Zhang YW; Tang HS; Li JX; Zhou XT
    Gynecol Obstet Invest; 1980; 11(1):17-36. PubMed ID: 7390274
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Female pseudohermaphroditism due to classical 21-hydroxylase deficiency in a girl with Turner syndrome.
    Maciel-Guerra AT; Guerra G; Marini SH; Matias Baptista MT; Marques-de-Faria AP
    Clin Genet; 1997 May; 51(5):351-3. PubMed ID: 9212186
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetically determined sex-reversal in 46,XY humans.
    German J; Simpson JL; Chaganti RS; Summitt RL; Reid LB; Merkatz IR
    Science; 1978 Oct; 202(4363):53-6. PubMed ID: 567843
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Pure gonadal dysgenesis in sisters].
    Chrz R; Málková J; Stárka L; Motlík K; Kobilková J; Macek M
    Sb Lek; 1972 Jul; 74(7):246-9. PubMed ID: 5050835
    [No Abstract]   [Full Text] [Related]  

  • 9. Pure gonadal dysgenesis (type XX). Report on a family with four affected sibs.
    Nazareth HR; Farah LM; Cunha AJ; Vieira FJ
    Hum Genet; 1977 Jun; 37(1):117-20. PubMed ID: 881190
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Swyer's syndrome (pure gonadal dysgenesis) and gonadal neoplasias in 3 sisters].
    Campodónico I; Venegas E; Saito E; Aspillaga M; Donoso S; Rodríguez A
    Rev Chil Obstet Ginecol; 1973; 38(4):155-64. PubMed ID: 4806784
    [No Abstract]   [Full Text] [Related]  

  • 11. Sex determination and gonadal differentiation in man. A unifying concept of normal and abnormal sex development.
    Boczkowski K
    Clin Genet; 1971; 2(6):379-86. PubMed ID: 5155315
    [No Abstract]   [Full Text] [Related]  

  • 12. [Swyer's syndrome (pure gonadal dysgenesis) and gonadal neoplasms in 3 sisters].
    Campodónico I; Venegas E; Saito E; Aspillaga M; Donoso S; Rodríguez A
    Rev Chil Obstet Ginecol; 1973; 38(4):155-64. PubMed ID: 4803561
    [No Abstract]   [Full Text] [Related]  

  • 13. [Turners syndrome in men].
    Zarubina NA; Glikman EV; Iur'eva NP
    Probl Endokrinol (Mosk); 1974; 20(4):29-34. PubMed ID: 4449796
    [No Abstract]   [Full Text] [Related]  

  • 14. Pure gonadal dysgenesis and ovarian dysplasia in sisters.
    Boczkowski K
    Am J Obstet Gynecol; 1970 Feb; 106(4):626-8. PubMed ID: 5412860
    [No Abstract]   [Full Text] [Related]  

  • 15. [Pure familial gonadal dysgenesis].
    Berger R; Binoux M; Chassan E; Lejeune J
    Ann Endocrinol (Paris); 1972; 33(1):35-40. PubMed ID: 4657311
    [No Abstract]   [Full Text] [Related]  

  • 16. ["Pure gonadal dysgenesis" with karyotype 44 A+XX in sisters, children of cousins].
    Giusti G; Borghi A; Salti M; Bigozzi U
    Acta Genet Med Gemellol (Roma); 1966 Jan; 15(1):51-68. PubMed ID: 5930172
    [No Abstract]   [Full Text] [Related]  

  • 17. [3 sisters with pure gonadal dysgenesis and XY karyotype].
    Stănesco V; Maximilian C; Florea I; Ciovîrnache M
    Ann Endocrinol (Paris); 1968; 29(4):449-59. PubMed ID: 5729505
    [No Abstract]   [Full Text] [Related]  

  • 18. [Pure familial gonadal dysgenesis and gonadoblastoma].
    Allard S; Cadotte M; Boivin Y
    Union Med Can; 1972 Mar; 101(3):448-52. PubMed ID: 5013462
    [No Abstract]   [Full Text] [Related]  

  • 19. 45,X/46,XY mosaicism: report of 27 cases.
    Telvi L; Lebbar A; Del Pino O; Barbet JP; Chaussain JL
    Pediatrics; 1999 Aug; 104(2 Pt 1):304-8. PubMed ID: 10429013
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.