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 *

156 related articles for article (PubMed ID: 10325262)

  • 1. Investigation of a unique male and female sibship with Kallmann's syndrome and 46,XX gonadal dysgenesis with short stature.
    Persson JW; Humphrey K; Watson C; Taylor P; Leigh D; McDonald B; Fraser IS
    Hum Reprod; 1999 May; 14(5):1207-12. PubMed ID: 10325262
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Kallmann's syndrome.
    Bouloux PM; Duke VM; Hall-Craggs M; Manning P; Quinton R; Jacobs HS
    Curr Opin Obstet Gynecol; 1994 Jun; 6(3):301-3. PubMed ID: 8038419
    [No Abstract]   [Full Text] [Related]  

  • 3. The Kallmann's syndrome variant (KSV) model of the schizophrenias.
    Cowen MA; Green M
    Schizophr Res; 1993 Mar; 9(1):1-10. PubMed ID: 8461265
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Xp22.3 deletions in isolated familial Kallmann's syndrome.
    Hardelin JP; Levilliers J; Young J; Pholsena M; Legouis R; Kirk J; Bouloux P; Petit C; Schaison G
    J Clin Endocrinol Metab; 1993 Apr; 76(4):827-31. PubMed ID: 8473391
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A case of hypogonadotrophic hypogonadism with anosmia (Kallmann's syndrome) in a male, with familial incidence of a small metacentric chromosome (47,XX, mat?+).
    Ventruto V; Cali A; Farina L; Festa B; Ricciardi I; Sebastio L
    J Med Genet; 1976 Feb; 13(1):71-5. PubMed ID: 1271431
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [X-linked Kallmann's syndrome: intra and interfamilial heterogeneity].
    Vidal A; Loidi L; Colino E; del Carmen Miranda M; Barrio R
    Med Clin (Barc); 2007 May; 128(20):777-9. PubMed ID: 17568506
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Short stature homeobox-containing gene duplication on the der(X) chromosome in a female with 45,X/46,X, der(X), gonadal dysgenesis, and tall stature.
    Ogata T; Kosho T; Wakui K; Fukushima Y; Yoshimoto M; Miharu N
    J Clin Endocrinol Metab; 2000 Aug; 85(8):2927-30. PubMed ID: 10946905
    [TBL] [Abstract][Full Text] [Related]  

  • 8. XY sex-reversed campomelia- possibly an X-linked disorder?
    Schimke RN
    Clin Genet; 1979 Jul; 16(1):62-3. PubMed ID: 477018
    [No Abstract]   [Full Text] [Related]  

  • 9. Gonadotropin-releasing hormone deficiency in the human (idiopathic hypogonadotropic hypogonadism and Kallmann's syndrome): pathophysiological and genetic considerations.
    Seminara SB; Hayes FJ; Crowley WF
    Endocr Rev; 1998 Oct; 19(5):521-39. PubMed ID: 9793755
    [No Abstract]   [Full Text] [Related]  

  • 10. Heterogeneity of Kallmann's syndrome.
    Hermanussen M; Sippell WG
    Clin Genet; 1985 Aug; 28(2):106-11. PubMed ID: 4042391
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Gonadal dysgenesis in a mother and her daughter (author's transl)].
    Riviere L; Serville F; Schmitt B; Roger P
    Ann Endocrinol (Paris); 1979; 40(4):427-8. PubMed ID: 518023
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of olfactory dysfunction in carriers of X-linked Kallmann's syndrome.
    Matfin G
    Clin Endocrinol (Oxf); 1995 May; 42(5):557-9. PubMed ID: 7621577
    [No Abstract]   [Full Text] [Related]  

  • 13. Multicystic dysplastic kidney and Kallmann's syndrome: a new association?
    Deeb A; Robertson A; MacColl G; Bouloux PM; Gibson M; Winyard PJ; Woolf AS; Moghal NE; Cheetham TD
    Nephrol Dial Transplant; 2001 Jun; 16(6):1170-5. PubMed ID: 11390716
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Gonadal dysgenesis and the X isochromosome].
    Szemere G; Szörényi AH; Szabó J
    Orv Hetil; 1983 Dec; 124(52):3151-3. PubMed ID: 6657259
    [No Abstract]   [Full Text] [Related]  

  • 15. [Balanced t(1;X) translocation in a woman with gonadal dysgenesis].
    Kirillova EA; Baranovskaia LI
    Genetika; 1982 Sep; 18(9):1544-9. PubMed ID: 6890495
    [No Abstract]   [Full Text] [Related]  

  • 16. [From gene to disease; hypogonatrophic hypogonadism and anosmia: Kallmann's syndrome].
    Voorhoeve PG; Delemarre-van de Waal HA
    Ned Tijdschr Geneeskd; 2004 Jun; 148(23):1142-4. PubMed ID: 15211964
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Gonadal dysgenesis with X-isochromosome of paternal origin (author's transl)].
    Zeitlhuber U; Frisch H; Schreibenreiter S
    Klin Padiatr; 1981 Sep; 193(5):390-1. PubMed ID: 7289433
    [No Abstract]   [Full Text] [Related]  

  • 18. Identification of olfactory dysfunction in carriers of X-linked Kallmann's syndrome.
    Kirk JM; Grant DB; Savage MO; Besser GM; Bouloux PM
    Clin Endocrinol (Oxf); 1994 Nov; 41(5):577-80. PubMed ID: 7828345
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A 48,XXXX female with absence of ovaries.
    Collen RJ; Falk RE; Lippe BM; Kaplan SA
    Am J Med Genet; 1980; 6(4):275-8. PubMed ID: 7211945
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Kallmann's syndrome.
    Kulkarni ML; Balaji MD; Kulkarni AM; Sushanth S; Kulkarni BM
    Indian J Pediatr; 2007 Dec; 74(12):1113-5. PubMed ID: 18174649
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.