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 *

128 related articles for article (PubMed ID: 1952792)

  • 21. Cytogenetics of müllerian agenesis. A case report.
    Jaffe SB; Loucopoulos A; Jewelewicz R
    J Reprod Med; 1992 Mar; 37(3):242-6. PubMed ID: 1564711
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Mosaicism 45,X/46,X, t dic(Xp:Xp) in a girl with short stature.
    Abulhasan SJ; Teebi AS; Zaki M; Hammad I; Al-Awadi SA; Krishna Murthy DS
    Ann Genet; 1990; 33(4):234-8. PubMed ID: 2095706
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Mosaic ring X chromosome in a case of secondary amenorrhea.
    Chrisoulidou A; Bili H; Georgiou E; Mavroudi S; Lazaridou AS
    Fertil Steril; 2008 Oct; 90(4):1198.e19-21. PubMed ID: 18177863
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Partial deletion of the short arm of the X chromosome in a patient with a monolateral ovarian streak].
    Simonetta R; Maraschio P
    Minerva Ginecol; 1984 Mar; 36(3):95-9. PubMed ID: 6728290
    [No Abstract]   [Full Text] [Related]  

  • 25. Report of a case of true hermaphroditism with karyotype 45,X/46,XX/46,X,mar/47,XX,mar.
    Kaluzewski B; Pawlikowski T; Moruzgala T; Reterski Z; Bjanid O
    J Genet Hum; 1977 Oct; 25(3):195-203. PubMed ID: 563432
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A case of long arm deletion of the X-chromosome in a patient with Turner syndrome.
    Maximilian C; Chirică S; Dumitriu L; Ciovîrnache M; Fabritius K; Pană I; Popa M; Ioan D
    Endocrinologie; 1983; 21(4):279-83. PubMed ID: 6665503
    [TBL] [Abstract][Full Text] [Related]  

  • 27. An X;9 translocation, primary amenorrhea, and hypothalamic dysfunction.
    Gardner HA; McConnon JK; MacKenzie MA
    Am J Med Genet; 1983 Apr; 14(4):647-56. PubMed ID: 6342391
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Gonadal dysgenesis and Rokitansky syndrome. A case report.
    Güitrón-Cantú A; López-Vera E; Forsbach-Sánchez G; Leal-Garza CH; Cortés-Gutiérrez EI; González-Pico I
    J Reprod Med; 1999 Oct; 44(10):891-3. PubMed ID: 10554753
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. [45,X/ 46,XX/ 46,XY Mosaic with female phenotype].
    Moreau N; Rochet Y; Peyramond C; Raymond D
    Bull Assoc Anat (Nancy); 1976 Dec; 60(171):757-67. PubMed ID: 1030251
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Clinical and hormonal studies in a male with karyotype 46,XX].
    Kumanow P; Beraha L
    Andrologia; 1983; 15(5):426-30. PubMed ID: 6418027
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Secondary amenorrhea associated with balanced X-autosome translocation.
    Sauer F; Greenstein RM; Reardon P; Riddick DH
    Obstet Gynecol; 1977 Jan; 49(1):101-4. PubMed ID: 831158
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Chromosomal complements in primary gonadal failure.
    Portuondo JA; Barral A; Melchor JC; Tanago JG; Neyro JL
    Obstet Gynecol; 1984 Dec; 64(6):757-61. PubMed ID: 6504419
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Delayed diagnosis in a case of secondary amenorrhea caused by a long arm isochromosome--X; i(xq).
    Kjessler B; Farhan M
    Int J Fertil; 1978; 23(4):305-8. PubMed ID: 33926
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Detection of triple X syndrome during a familial inquiry for hemophilia A].
    Plaisancie H; Bourrouillou G; Calvas P; Colombies P
    J Genet Hum; 1989 Jun; 37(2):149-53. PubMed ID: 2568388
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The phenotypic effects of small, distal Xq deletions.
    Trunca C; Therman E; Rosenwaks Z
    Hum Genet; 1984; 68(1):87-9. PubMed ID: 6500561
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Ullrich-Turner syndrome associated with interstitial deletion of Xp11.4 leads to p22.31.
    Wilson MG; Modebe O; Towner JW; Frasier SD; Lin MS
    Am J Med Genet; 1983 Mar; 14(3):567-76. PubMed ID: 6859107
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Sex chromosome disorders.
    Pitcher D
    Crit Rev Clin Lab Sci; 1981; 13(4):241-82. PubMed ID: 7016435
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Coexistence of gonadal dysgenesis and Mullerian agenesis with two mosaic cell lines 45,X/46,X,del(X)(p22.2).
    Ting TC; Chang SP
    Zhonghua Yi Xue Za Zhi (Taipei); 2002 Sep; 65(9):450-2. PubMed ID: 12433033
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.