146 related articles for article (PubMed ID: 36416214)
1. SOX3 duplication in a boy with 46,XX ovotesticular disorder of sex development and his 46,XX sister with atypical genitalia: Probable germline mosaicism.
de Oliveira FM; Barros BA; Dos Santos AP; Campos NLV; Mazzola TN; Filho PL; Andrade LALA; Guaragna MS; de Mello MP; Guerra-Junior G; Vieira TAP; Maciel-Guerra AT
Am J Med Genet A; 2023 Feb; 191(2):592-598. PubMed ID: 36416214
[TBL] [Abstract][Full Text] [Related]
2. 46,XX ovotesticular DSD associated with a SOX3 gene duplication in a SRY-negative boy.
Grinspon RP; Nevado J; Mori Alvarez Mde L; Del Rey G; Castera R; Venara M; Chiesa A; Podestá M; Lapunzina P; Rey RA
Clin Endocrinol (Oxf); 2016 Oct; 85(4):673-5. PubMed ID: 27260338
[No Abstract] [Full Text] [Related]
3. A Duplication Upstream of SOX9 Associated with
Mengen E; Kayhan G; Kocaay P; Uçaktürk SA
J Clin Res Pediatr Endocrinol; 2020 Sep; 12(3):308-314. PubMed ID: 31476840
[TBL] [Abstract][Full Text] [Related]
4. Are NR5A1 Variations a Frequent Cause of 46,XX Ovotesticular Disorders of Sex Development? Analysis from a Single Center and Systematic Review.
Barros BA; Guaragna MS; Fabbri-Scallet H; Palandi de Mello M; Guerra-Júnior G; Maciel-Guerra AT
Sex Dev; 2022; 16(4):242-251. PubMed ID: 36657429
[TBL] [Abstract][Full Text] [Related]
5. Whole genome sequencing identifies a cryptic SOX9 regulatory element duplication underlying a case of 46,XX ovotesticular difference of sexual development.
Qian Z; Grand K; Freedman A; Nieto MC; Behlmann A; Schweiger BM; Sanchez-Lara PA
Am J Med Genet A; 2021 Sep; 185(9):2782-2788. PubMed ID: 34050715
[TBL] [Abstract][Full Text] [Related]
6. The 46, XX Ovotesticular Disorder of Sex Development With Xq27.1q27.2 Duplication Involving the
Zhuang J; Chen C; Li J; Jiang Y; Wang J; Wang Y; Zeng S; Lin Y; Xie Y
Front Pediatr; 2021; 9():682846. PubMed ID: 34178900
[No Abstract] [Full Text] [Related]
7. Duplication of SOX3 in an SRY-negative 46,XX male with prostatic utricle: case report and literature review.
Wei J; Liu C; Zhang M; Liu S; Fu J; Lin P
BMC Med Genomics; 2022 Sep; 15(1):188. PubMed ID: 36064700
[TBL] [Abstract][Full Text] [Related]
8. Duplication of SOX9 is not a common cause of 46,XX testicular or 46,XX ovotesticular DSD.
Seeherunvong T; Ukarapong S; McElreavey K; Berkovitz GD; Perera EM
J Pediatr Endocrinol Metab; 2012; 25(1-2):121-3. PubMed ID: 22570960
[TBL] [Abstract][Full Text] [Related]
9. Partial deletion of DMRT1 causes 46,XY ovotesticular disorder of sexual development.
Ledig S; Hiort O; Wünsch L; Wieacker P
Eur J Endocrinol; 2012 Jul; 167(1):119-24. PubMed ID: 22573722
[TBL] [Abstract][Full Text] [Related]
10. A 46,XX Ovotesticular Disorder of Sex Development Likely Caused by a Steroidogenic Factor-1 (NR5A1) Variant.
Swartz JM; Ciarlo R; Guo MH; Abrha A; Weaver B; Diamond DA; Chan YM; Hirschhorn JN
Horm Res Paediatr; 2017; 87(3):191-195. PubMed ID: 27855412
[TBL] [Abstract][Full Text] [Related]
11. The smallest dislocated microduplication of Xq27.1 harboring
Oroz M; Vičić A; Požgaj Šepec M; Karnaš H; Stipančić G; Stipoljev F
J Pediatr Endocrinol Metab; 2023 Jan; 36(1):86-90. PubMed ID: 36189645
[TBL] [Abstract][Full Text] [Related]
12. Duplication of SOX9 associated with 46,XX ovotesticular disorder of sex development.
López-Hernández B; Méndez JP; Coral-Vázquez RM; Benítez-Granados J; Zenteno JC; Villegas-Ruiz V; Calzada-León R; Soderlund D; Canto P
Reprod Biomed Online; 2018 Jul; 37(1):107-112. PubMed ID: 29673731
[TBL] [Abstract][Full Text] [Related]
13. Ovotesticular disorder of sexual development and a rare 46,XX/47,XXY karyotype.
Ozsu E; Mutlu GY; Cizmecioglu FM; Ekingen G; Muezzinoglu B; Hatun S
J Pediatr Endocrinol Metab; 2013; 26(7-8):789-91. PubMed ID: 23612643
[TBL] [Abstract][Full Text] [Related]
14. Testis development in the absence of SRY: chromosomal rearrangements at SOX9 and SOX3.
Vetro A; Dehghani MR; Kraoua L; Giorda R; Beri S; Cardarelli L; Merico M; Manolakos E; Parada-Bustamante A; Castro A; Radi O; Camerino G; Brusco A; Sabaghian M; Sofocleous C; Forzano F; Palumbo P; Palumbo O; Calvano S; Zelante L; Grammatico P; Giglio S; Basly M; Chaabouni M; Carella M; Russo G; Bonaglia MC; Zuffardi O
Eur J Hum Genet; 2015 Aug; 23(8):1025-32. PubMed ID: 25351776
[TBL] [Abstract][Full Text] [Related]
15. Gonadoblastoma and Papillary Tubal Hyperplasia in Ovotesticular Disorder of Sexual Development.
Şimşek E; Binay Ç; Demiral M; Tokar B; Kabukçuoğlu S; Üstün M
J Clin Res Pediatr Endocrinol; 2016 Sep; 8(3):351-5. PubMed ID: 27087521
[TBL] [Abstract][Full Text] [Related]
16. Methylation Patterns of SOX3, SOX9, and WNT4 Genes in Gonads of Dogs with XX (SRY-Negative) Disorder of Sexual Development.
Salamon S; Flisikowski K; Switonski M
Sex Dev; 2017; 11(2):86-93. PubMed ID: 28365713
[TBL] [Abstract][Full Text] [Related]
17. Female-to-male sex reversal associated with unique Xp21.2 deletion disrupting genomic regulatory architecture of the dosage-sensitive sex reversal region.
Dangle P; Touzon MS; Reyes-Múgica M; Witchel SF; Rajkovic A; Schneck FX; Yatsenko SA
J Med Genet; 2017 Oct; 54(10):705-709. PubMed ID: 28483799
[TBL] [Abstract][Full Text] [Related]
18. Duplication of The
Tasic V; Mitrotti A; Riepe FG; Kulle AE; Laban N; Polenakovic M; Plaseska-Karanfilska D; Sanna-Cherchi S; Kostovski M; Gucev Z
Balkan J Med Genet; 2019 Jun; 22(1):81-88. PubMed ID: 31523625
[TBL] [Abstract][Full Text] [Related]
19. SRY-negative 46,XX testicular/ovotesticular DSD: Long-term outcomes and early blockade of gonadotropic axis.
Lambert S; Peycelon M; Samara-Boustani D; Hyon C; Dumeige L; Peuchmaur M; Fiot E; Léger J; Simon D; Paye-Jaouen A; Bouligand J; Siffroi JP; Carel JC; McElreavey K; El Ghoneimi A; Brachet C; Bouvattier C; Martinerie L
Clin Endocrinol (Oxf); 2021 Apr; 94(4):667-676. PubMed ID: 33296530
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
