252 related articles for article (PubMed ID: 29618062)
21. 46, XY gonadal dysgenesis: new SRY point mutation in two siblings with paternal germ line mosaicism.
Stoppa-Vaucher S; Ayabe T; Paquette J; Patey N; Francoeur D; Vuissoz JM; Deladoëy J; Samuels ME; Ogata T; Deal CL
Clin Genet; 2012 Dec; 82(6):505-13. PubMed ID: 22288726
[TBL] [Abstract][Full Text] [Related]
22. Report of a kindred with X-linked (or autosomal dominant sex-limited) 46,XY partial gonadal dysgenesis.
Fechner PY; Marcantonio SM; Ogata T; Rosales TO; Smith KD; Goodfellow PN; Migeon CJ; Berkovitz GD
J Clin Endocrinol Metab; 1993 May; 76(5):1248-53. PubMed ID: 8496317
[TBL] [Abstract][Full Text] [Related]
23. 45,X/46,XY mosaicism: report of 27 cases.
Telvi L; Lebbar A; Del Pino O; Barbet JP; Chaussain JL
Pediatrics; 1999 Aug; 104(2 Pt 1):304-8. PubMed ID: 10429013
[TBL] [Abstract][Full Text] [Related]
24. The clinical and genetic heterogeneity of mixed gonadal dysgenesis: does "disorders of sexual development (DSD)" classification based on new Chicago consensus cover all sex chromosome DSD?
Ocal G; Berberoğlu M; Sıklar Z; Ruhi HI; Tükün A; Camtosun E; Savaş Erdeve S; Hacıhamdioğlu B; Fitöz S
Eur J Pediatr; 2012 Oct; 171(10):1497-502. PubMed ID: 22644991
[TBL] [Abstract][Full Text] [Related]
25. Clinical heterogeneity in children with gonadal dysgenesis associated with non-mosaic 46,XY karyotype.
Wong YS; Tam YH; Pang KKY; To KF; Chan SSC; Chan KW; Lee KH
J Pediatr Urol; 2017 Oct; 13(5):508.e1-508.e6. PubMed ID: 28434637
[TBL] [Abstract][Full Text] [Related]
26. 45,X/46,XY mosaicism: a cause of short stature in males.
Efthymiadou A; Stefanou EG; Chrysis D
Hormones (Athens); 2012; 11(4):501-4. PubMed ID: 23422775
[TBL] [Abstract][Full Text] [Related]
27. [Pure 46,XY gonadal dysgenesis].
Ságodi L; Ladányi E; Kiss Á; Tar A; Lukács V; Minik K; Vámosi I
Orv Hetil; 2010 Nov; 151(48):1991-5. PubMed ID: 21084251
[TBL] [Abstract][Full Text] [Related]
28. Clinical aspects of 49 infertile males with 45,X/46,XY mosaicism karyotype: A case series.
Mohammadpour Lashkari F; Sadighi Gilani MA; Ghaheri A; Zamanian MR; Borjian Boroujeni P; Mohseni Meybodi A; Sabbaghian M
Andrologia; 2018 Jun; 50(5):e13009. PubMed ID: 29527714
[TBL] [Abstract][Full Text] [Related]
29. [Pathologic features on gonadal changes of sexual developmental disorders in children].
Yi P; Niu HL; Gao Q; Wang FH; Jia W; Chen ZR; Xia JQ; Li LP; Cao Y; Zeng RX
Zhonghua Bing Li Xue Za Zhi; 2018 Jul; 47(7):531-535. PubMed ID: 29996319
[No Abstract] [Full Text] [Related]
30. A phenotypic male with true hermaphroditism and a 46,XX/46,XY/47,XXY karyotype.
Wit JM; Quartero AO; Bax NM; Huber J
Clin Genet; 1987 Apr; 31(4):243-8. PubMed ID: 3594931
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Description of diagnosis of 45,X/46,XY ovotesticular DSD.
Ren Š; Harmaš V; Stará M; Laštůvkováj ; Čejnová V
Ceska Gynekol; 2020; 85(4):259-262. PubMed ID: 33562981
[TBL] [Abstract][Full Text] [Related]
33. True hermaphroditism: genetic variants and clinical management.
Hadjiathanasiou CG; Brauner R; Lortat-Jacob S; Nivot S; Jaubert F; Fellous M; Nihoul-Fékété C; Rappaport R
J Pediatr; 1994 Nov; 125(5 Pt 1):738-44. PubMed ID: 7965425
[TBL] [Abstract][Full Text] [Related]
34. Natural history and long-term testicular growth of acquired undescended testis after spontaneous descent or pubertal orchidopexy.
Hack WW; van der Voort-Doedens LM; Goede J; van Dijk JM; Meijer RW; Sijstermans K
BJU Int; 2010 Oct; 106(7):1052-9. PubMed ID: 20151964
[TBL] [Abstract][Full Text] [Related]
35. [Causes of ambiguous external genitalia in neonates].
Zdravković D; Milenković T; Sedlecki K; Guć-Sćekić M; Rajić V; Banićević M
Srp Arh Celok Lek; 2001; 129(3-4):57-60. PubMed ID: 11534268
[TBL] [Abstract][Full Text] [Related]
36. Long-term follow-up and analysis of monozygotic twins concordant for 45,X/46,XY peripheral blood karyotype but discordant for phenotypic sex.
Tho SP; Jackson R; Kulharya AS; Reindollar RH; Layman LC; McDonough PG
Am J Med Genet A; 2007 Nov; 143A(21):2616-22. PubMed ID: 17935253
[TBL] [Abstract][Full Text] [Related]
37. Familial forms of disorders of sex development may be common if infertility is considered a comorbidity.
Brauner R; Picard-Dieval F; Lottmann H; Rouget S; Bignon-Topalovic J; Bashamboo A; McElreavey K
BMC Pediatr; 2016 Nov; 16(1):195. PubMed ID: 27899089
[TBL] [Abstract][Full Text] [Related]
38. [Diagnosis and management of 46,XY mixed gonadal dysgenesis and disorder of sexual differentiation].
Verkauskas G; Macianskyte D; Janciauskas D; Preiksa RT; Verkauskiene R; Jaubert F
Medicina (Kaunas); 2009; 45(5):357-64. PubMed ID: 19535881
[TBL] [Abstract][Full Text] [Related]
39. Clinical but Not Histological Outcomes in Males With 45,X/46,XY Mosaicism Vary Depending on Reason for Diagnosis.
Ljubicic ML; Jørgensen A; Acerini C; Andrade J; Balsamo A; Bertelloni S; Cools M; Cuccaro RT; Darendeliler F; Flück CE; Grinspon RP; Maciel-Guerra A; Guran T; Hannema SE; Lucas-Herald AK; Hiort O; Holterhus PM; Lichiardopol C; Looijenga LHJ; Ortolano R; Riedl S; Ahmed SF; Juul A
J Clin Endocrinol Metab; 2019 Oct; 104(10):4366-4381. PubMed ID: 31127831
[TBL] [Abstract][Full Text] [Related]
40. Case Report: Longitudinal follow-up and testicular sperm extraction in a patient with a pathogenic
Teoli J; Mallet D; Renault L; Gay CL; Labrune E; Bretones P; Giscard D'Estaing S; Cuzin B; Dijoud F; Roucher-Boulez F; Plotton I
Front Endocrinol (Lausanne); 2023; 14():1171822. PubMed ID: 37409232
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]