334 related articles for article (PubMed ID: 30017534)
41. The use of fluorescence in situ hybridization in the diagnosis of hidden mosaicism: apropos of three cases of sex chromosome anomalies.
Maciel-Guerra AT; Paulo JD; Santos AP; Guaragna-Filho G; Andrade JG; Siviero-Miachon AA; Spinola-Castro AM; Guerra-Júnior G
Arq Bras Endocrinol Metabol; 2012 Nov; 56(8):545-51. PubMed ID: 23295296
[TBL] [Abstract][Full Text] [Related]
42. The role of SRY mutations in the etiology of gonadal dysgenesis in patients with 45,X/46,XY disorder of sex development and variants.
Nishi MY; Costa EM; Oliveira SB; Mendonca BB; Domenice S
Horm Res Paediatr; 2011; 75(1):26-31. PubMed ID: 20699606
[TBL] [Abstract][Full Text] [Related]
43. Mixed gonadal dysgenesis and sex chromosome mosaicism with multiple cell lines including structural aberrations of the Y chromosome.
Al-Awadi SA; Cuschieri A; Farag TI; Naguib K; Teebi AS; Issa M; El-Sayed M
Clin Genet; 1983 Feb; 23(2):172-6. PubMed ID: 6682358
[TBL] [Abstract][Full Text] [Related]
44. Early Bilateral Gonadoblastoma in a Patient with Mixed Gonadal Dysgenesis (Karyotype 45,X/46,XY): Case Report and Review of Literature.
Trainavičius I; Dasevičius D; Burnytė B; Kemežys R; Verkauskas G
Acta Med Litu; 2022; 29(2):194-200. PubMed ID: 37733428
[TBL] [Abstract][Full Text] [Related]
45. Mixed gonadal dysgenesis with 45,X/46,X,idic(Y)/46,XY,idic(Y) karyotype.
Caglayan AO; Demiryilmaz F; Kendirci M; Ozyazgan I; Akalin H; Bittmann S
Genet Couns; 2009; 20(2):173-9. PubMed ID: 19650415
[TBL] [Abstract][Full Text] [Related]
46. Mixed gonadal dysgenesis: a syndrome of broad clinical, cytogenetic and histopathologic spectrum.
Alvarez-Nava F; Gonzalez S; Soto S; Pineda L; Morales-Machin A
Genet Couns; 1999; 10(3):233-43. PubMed ID: 10546094
[TBL] [Abstract][Full Text] [Related]
47. Growth in Boys with 45,X/46,XY Mosaicism: Effect of Growth Hormone Treatment on Statural Growth.
Bertelloni S; Baroncelli GI; Massart F; Toschi B
Sex Dev; 2015; 9(4):183-9. PubMed ID: 26529521
[TBL] [Abstract][Full Text] [Related]
48. Video-assisted gonadectomy in children with Ullrich Turner syndrome or 46,XY gonadal dysgenesis.
Tröbs RB; Hoepffner W; Bühligen U; Limbach A; Keller E; Schütz A; Horn LC; Kiess W; Bennek J
Eur J Pediatr Surg; 2004 Jun; 14(3):179-84. PubMed ID: 15211408
[TBL] [Abstract][Full Text] [Related]
49. Phenotypic spectrum of 45,X/46,XY individuals.
Rosenberg C; Frota-Pessoa O; Vianna-Morgante AM; Chu TH
Am J Med Genet; 1987 Jul; 27(3):553-9. PubMed ID: 3631129
[TBL] [Abstract][Full Text] [Related]
50. Gonadoblastoma and Turner syndrome.
Brant WO; Rajimwale A; Lovell MA; Travers SH; Furness PD; Sorensen M; Oottamasathien S; Koyle MA
J Urol; 2006 May; 175(5):1858-60. PubMed ID: 16600779
[TBL] [Abstract][Full Text] [Related]
51. Undetectable anti-Mullerian hormone and inhibin B do not preclude the presence of germ cell tumours in 45,X/46,XY or 46,XY gonadal dysgenesis.
Hannema SE; Wolffenbuttel KP; van Bever Y; Brüggenwirth HT; van den Berg SAA; Hersmus R; Oosterhuis JW; Looijenga LHJ
Clin Endocrinol (Oxf); 2023 Jul; 99(1):58-63. PubMed ID: 36905105
[TBL] [Abstract][Full Text] [Related]
52. Gonadal mosaicism 45,X/46,X,psu dic(Y)(q11.2) resulting in a Turner phenotype with mixed gonadal dysgenesis.
Gole LA; Lim J; Crolla JA; Loke KY
Singapore Med J; 2008 Apr; 49(4):349-51. PubMed ID: 18418530
[TBL] [Abstract][Full Text] [Related]
53. Gonadal pathology and tumor risk in relation to clinical characteristics in patients with 45,X/46,XY mosaicism.
Cools M; Pleskacova J; Stoop H; Hoebeke P; Van Laecke E; Drop SL; Lebl J; Oosterhuis JW; Looijenga LH; Wolffenbuttel KP;
J Clin Endocrinol Metab; 2011 Jul; 96(7):E1171-80. PubMed ID: 21508138
[TBL] [Abstract][Full Text] [Related]
54. Gonadal tumour risk in 292 phenotypic female patients with disorders of sex development containing Y chromosome or Y-derived sequence.
Huang H; Wang C; Tian Q
Clin Endocrinol (Oxf); 2017 Apr; 86(4):621-627. PubMed ID: 27862157
[TBL] [Abstract][Full Text] [Related]
55. A Case of 45,X/46,XY Mosaicism Presenting as Swyer Syndrome.
Chand MT; Turner S; Solomon LA; Jay A; Rabah R; Misra VK
J Pediatr Adolesc Gynecol; 2020 Oct; 33(5):577-580. PubMed ID: 32565348
[TBL] [Abstract][Full Text] [Related]
56. Mixed gonadal dysgenesis and dysgenetic male pseudohermaphroditism--a critical analysis.
Rohatgi M; Gupta DK; Menon PS; Verma IC; Mathur M
Indian J Pediatr; 1992; 59(4):487-500. PubMed ID: 1452268
[TBL] [Abstract][Full Text] [Related]
57. Gonadoblastoma in patients with Ullrich-Turner syndrome.
Zelaya G; López Marti JM; Marino R; Garcia de Dávila MT; Gallego MS
Pediatr Dev Pathol; 2015; 18(2):117-21. PubMed ID: 25535833
[TBL] [Abstract][Full Text] [Related]
58. 45,X mosaicism with Y chromosome presenting female phenotype.
Fukui S; Watanabe M; Yoshino K
J Pediatr Surg; 2015 Jul; 50(7):1220-3. PubMed ID: 26002715
[TBL] [Abstract][Full Text] [Related]
59. Dysgenetic male pseudohermaphroditism in a 45,X/46,X,del(Y)(q11.1) mosaic infant.
Gaba AR; Van Dyke DL; Weiss L
Am J Med Genet; 1987 Mar; 26(3):545-9. PubMed ID: 3565468
[TBL] [Abstract][Full Text] [Related]
60. [The use of FISH on buccal smear to investigate mosaicism with a 45,X cell line: study on healthy men and patients with disorders of sex development].
Paulo Jd; Andrade JG; Santos AP; Gil-da-Silva-Lopes VL; Guerra-Júnior G; Maciel-Guerra AT
Arq Bras Endocrinol Metabol; 2014 Jun; 58(4):328-34. PubMed ID: 24936726
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]