BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

133 related articles for article (PubMed ID: 1329488)

  • 1. End-stage renal disease and primary hypogonadism associated with a 46,XX karyotype.
    Bailey WA; Zwingman TA; Reznik VM; Griswold WR; Mendoza SA; Jones KL; Freidenberg GR
    Am J Dis Child; 1992 Oct; 146(10):1218-23. PubMed ID: 1329488
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical and anatomical spectrum in XX sex reversed patients. Relationship to the presence of Y specific DNA-sequences.
    Boucekkine C; Toublanc JE; Abbas N; Chaabouni S; Ouahid S; Semrouni M; Jaubert F; Toublanc M; McElreavey K; Vilain E
    Clin Endocrinol (Oxf); 1994 Jun; 40(6):733-42. PubMed ID: 8033363
    [TBL] [Abstract][Full Text] [Related]  

  • 3. XY gonadal dysgenesis in an adolescent with chronic renal failure: a case of Frasier syndrome.
    Murray SC
    J Pediatr Adolesc Gynecol; 1998 May; 11(2):89-91. PubMed ID: 9593608
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Evaluation of delayed puberty in the female adolescent with chronic renal failure.
    Reznik VM; Mendoza SA; Freidenberg GR
    Pediatr Nephrol; 1993 Oct; 7(5):551-3. PubMed ID: 8251320
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Minimal external masculinization in a SRY-negative XX male Podenco dog.
    Buijtels JJ; de Gier J; van Haeften T; Kooistra HS; Spee B; Veldhuis Kroeze EJ; Zijlstra C; Okkens AC
    Reprod Domest Anim; 2009 Oct; 44(5):751-6. PubMed ID: 18992091
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Disorders of sexual development and associated changes in the pituitary-gonadal axis in dogs.
    Buijtels JJ; de Gier J; Kooistra HS; Grinwis GC; Naan EC; Zijlstra C; Okkens AC
    Theriogenology; 2012 Oct; 78(7):1618-26. PubMed ID: 22980090
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Chromosomally competent ovarian failure at adolescence.
    Rauh JL; Waldrop CD; Burket RL
    J Adolesc Health Care; 1983 Dec; 4(4):257-60. PubMed ID: 6315654
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Clinical, molecular and cytogenetic studies on 4 patients with 46, XX (SRY positive) male syndrome].
    Xia XY; Cui YX; Lu HY; Yang B; Wang GH; Pan LJ; Hou BS; Ge YF; Shao Y; Yao B; Huang YF
    Zhonghua Nan Ke Xue; 2007 Dec; 13(12):1094-7. PubMed ID: 18284058
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 46,XX gonadal dysgenesis, short stature, and recurrent metabolic acidosis in two sisters.
    Hisama FM; Zemel S; Cherniske EM; Vladutiu GD; Pober BR
    Am J Med Genet; 2001 Jan; 98(2):121-4. PubMed ID: 11223846
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Deletion of the Sry region on the Y chromosome detected in a case of equine gonadal hypoplasia (XY female) with abnormal hormonal profiles.
    Abe S; Miyake YI; Kageyama SI; Watanabe G; Taya K; Kawakura K
    Equine Vet J; 1999 Jul; 31(4):336-8. PubMed ID: 10454094
    [No Abstract]   [Full Text] [Related]  

  • 11. [Gonadal dysgenesis in own material].
    Gasińska-Drozdowska I; Goluda M; Hirowska-Tracz M; Roszyk-Rybińska A
    Ginekol Pol; 1999 May; 70(5):363-6. PubMed ID: 10462982
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A syndrome of female pseudohermaphrodism, hypergonadotropic hypogonadism, and multicystic ovaries associated with missense mutations in the gene encoding aromatase (P450arom).
    Conte FA; Grumbach MM; Ito Y; Fisher CR; Simpson ER
    J Clin Endocrinol Metab; 1994 Jun; 78(6):1287-92. PubMed ID: 8200927
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Familial 46,XX gonadal dysgenesis.
    Portuondo JA; Neyro JL; Benito JA; de los Rios A; Barral A
    Int J Fertil; 1987; 32(1):56-8. PubMed ID: 2880817
    [TBL] [Abstract][Full Text] [Related]  

  • 14. XX Maleness and XX true hermaphroditism in SRY-negative monozygotic twins: additional evidence for a common origin.
    Maciel-Guerra AT; de Mello MP; Coeli FB; Ribeiro ML; Miranda ML; Marques-de-Faria AP; Baptista MT; Moraes SG; Guerra-Júnior G
    J Clin Endocrinol Metab; 2008 Feb; 93(2):339-43. PubMed ID: 18056774
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Ovotesticular disorder of sexual development due to 47,XYY/46,XY/45,X mixed gonadal dysgenesis in a phenotypic male presenting as cyclical haematuria: clinical presentation and assessment of long-term outcomes.
    Dutta D; Shivaprasad KS; Das RN; Ghosh S; Chatterjee U; Chowdhury S; Dasgupta R
    Andrologia; 2014 Mar; 46(2):191-3. PubMed ID: 23163819
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [De La Chapelle syndrome].
    Dupuy O; Palou M; Mayaudon H; Sarret D; Bordier L; Garcin JM; Bauduceau B
    Presse Med; 2001 Mar; 30(8):369-72. PubMed ID: 11268892
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ontogeny of gonadotropin secretion in congenital anorchism: sexual dimorphism versus syndrome of gonadal dysgenesis and diagnostic considerations.
    Lustig RH; Conte FA; Kogan BA; Grumbach MM
    J Urol; 1987 Sep; 138(3):587-91. PubMed ID: 3114503
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 46,XX gonadal absence: a variant of the XX pure gonadal dysgenesis?
    Medina M; Kofman-Alfaro S; Pérez-Palacios G
    Acta Endocrinol (Copenh); 1982 Apr; 99(4):585-7. PubMed ID: 6803492
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Case of ovarian dysgenesis and dilated cardiomyopathy supports existence of Malouf syndrome.
    Narahara K; Kamada M; Takahashi Y; Tsuji K; Yokoyama Y; Ninomiya S; Seino Y
    Am J Med Genet; 1992 Oct; 44(3):369-73. PubMed ID: 1488988
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Pituitary-gonadal function in Klinefelter syndrome before and during puberty.
    Salbenblatt JA; Bender BG; Puck MH; Robinson A; Faiman C; Winter JS
    Pediatr Res; 1985 Jan; 19(1):82-6. PubMed ID: 3918293
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.