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7. [Secondary amenorrhoea and translocation between the X and 1 chromosome. The importance of the place where the break occurs (author's transl)]. Fournier JP; Gagnaire JC; Noël B J Gynecol Obstet Biol Reprod (Paris); 1981; 10(6):573-8. PubMed ID: 7320451 [No Abstract] [Full Text] [Related]
8. Trisomy 8p by malsegregation of a t(5;8)(p15;p11)mat in a case of XY pure gonadal dysgenesis. Memo L; Lenzini E; Baccichetti C Ann Genet; 1988; 31(3):181-5. PubMed ID: 3066281 [TBL] [Abstract][Full Text] [Related]
9. Gonadal dysgenesis in a patient with an X;3 translocation: case report and review. Carpenter NJ; Say B; Browning D J Med Genet; 1980 Jun; 17(3):216-21. PubMed ID: 7401133 [TBL] [Abstract][Full Text] [Related]
10. Cytogenetic and clinical studies in gonadal dysgenesis with 46,X,Xt(qter leads to p221::p223 leads to qter) karyotype: review and phenotype/karyotype correlations. Ferraro M; De Capoa A; Mostacci C; Pelliccia F; Zulli P; Baldini MA; Di Nisio Q J Med Genet; 1980 Dec; 17(6):457-63. PubMed ID: 7205428 [TBL] [Abstract][Full Text] [Related]
11. [Pure ovarian dysgenesis with translocation t (X;3) (q21;q12) (author's transl)]. Mariani R; Lambert JC; Krebs B; Depaz G; Ayraud N Ann Pediatr (Paris); 1980 Feb; 27(2):129-32. PubMed ID: 7425465 [No Abstract] [Full Text] [Related]
12. Disruption of friend of GATA 2 gene (FOG-2) by a de novo t(8;10) chromosomal translocation is associated with heart defects and gonadal dysgenesis. Finelli P; Pincelli AI; Russo S; Bonati MT; Recalcati MP; Masciadri M; Giardino D; Cavagnini F; Larizza L Clin Genet; 2007 Mar; 71(3):195-204. PubMed ID: 17309641 [TBL] [Abstract][Full Text] [Related]
13. Premature ovarian failure and ovarian dysgenesis associated with balanced and unbalanced X-6 translocations, respectively: implications for the investigation of ovarian failure. Center JR; McElduff A; Roberts CG Aust N Z J Obstet Gynaecol; 1994 May; 34(2):185-8. PubMed ID: 7980310 [TBL] [Abstract][Full Text] [Related]
14. Gonadal dysgenesis in del(18p) syndrome. Telvi L; Bernheim A; Ion A; Fouquet F; Le Bouc Y; Chaussain JL Am J Med Genet; 1995 Jul; 57(4):598-600. PubMed ID: 7573136 [TBL] [Abstract][Full Text] [Related]
15. Amenorrhea in gonadal dysgenesis, caused by chromosomal translocation. Gedda L; Carrega R; Borgese L; Strollo F Acta Genet Med Gemellol (Roma); 1995; 44(1):1-7. PubMed ID: 7653199 [TBL] [Abstract][Full Text] [Related]
16. [46,x,t(x;15)(q21;q22) gonadal dysgenesis]. Aritaki S; Someya H; Ogihara M; Ushio M; Matsuno T Horumon To Rinsho; 1983 Jun; 31 Suppl():59-62. PubMed ID: 6616923 [No Abstract] [Full Text] [Related]
17. Structural aberration of the X chromosome in a patient with gonadal dysgenesis: an approach to karyotype-phenotype correlation. Varella-Garcia M; Tajara EH; Gagliardi AR J Med Genet; 1981 Jun; 18(3):228-31. PubMed ID: 7241547 [TBL] [Abstract][Full Text] [Related]
18. An infant with a mosaic 45,X/46,X,psu dic(Y) (pter-->q11.2::q11.2-->pter) karyotype and mixed gonadal dysgenesis studied for extent of mosaicism in the gonads. Reddy KS; Sulcova V; Ho CK; Conner ED; Khurana A Am J Med Genet; 1996 Dec; 66(4):441-4. PubMed ID: 8989464 [TBL] [Abstract][Full Text] [Related]
19. [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]
20. Gonadal dysgenesis and the Mayer-Rokitansky-Kuster-Hauser syndrome in a girl with 46,X,del(X)(pter-->q22:). Aydos S; Tükün A; Bökesoy I Arch Gynecol Obstet; 2003 Jan; 267(3):173-4. PubMed ID: 12552332 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]