159 related articles for article (PubMed ID: 29219112)
41. Haploinsufficiency and triploinsensitivity of the same 6p25.1p24.3 region in a family.
Qi Z; Jeng LJ; Slavotinek A; Yu J
BMC Med Genomics; 2015 Jul; 8():38. PubMed ID: 26174853
[TBL] [Abstract][Full Text] [Related]
42. 46,XX testicular disorder of sexual development with SRY-negative caused by some unidentified mechanisms: a case report and review of the literature.
Li TF; Wu QY; Zhang C; Li WW; Zhou Q; Jiang WJ; Cui YX; Xia XY; Shi YC
BMC Urol; 2014 Dec; 14():104. PubMed ID: 25529318
[TBL] [Abstract][Full Text] [Related]
43. Ovotesticular Disorders of Sex Development: Improvement in Spermatogonia after Removal of Ovary and Müllerian Structures.
Abd Wahab AV; Lim LM; Mohamed Tarmizi MH
J Pediatr Adolesc Gynecol; 2019 Feb; 32(1):74-77. PubMed ID: 30248506
[TBL] [Abstract][Full Text] [Related]
44. Hypospadias in a male (78,XY; SRY-positive) dog and sex reversal female (78,XX; SRY-negative) dogs: clinical, histological and genetic studies.
Switonski M; Payan-Carreira R; Bartz M; Nowacka-Woszuk J; Szczerbal I; Colaço B; Pires MA; Ochota M; Nizanski W
Sex Dev; 2012; 6(1-3):128-34. PubMed ID: 21893969
[TBL] [Abstract][Full Text] [Related]
45. Extended pedigree with multiple cases of XX sex reversal in the absence of SRY and of a mutation at the SOX9 locus.
Temel SG; Gulten T; Yakut T; Saglam H; Kilic N; Bausch E; Jin WJ; Leipoldt M; Scherer G
Sex Dev; 2007; 1(1):24-34. PubMed ID: 18391513
[TBL] [Abstract][Full Text] [Related]
46. Genetic mutations and somatic anomalies in association with 46,XY gonadal dysgenesis.
Bastian C; Muller JB; Lortat-Jacob S; Nihoul-Fékété C; Bignon-Topalovic J; McElreavey K; Bashamboo A; Brauner R
Fertil Steril; 2015 May; 103(5):1297-304. PubMed ID: 25813279
[TBL] [Abstract][Full Text] [Related]
47. A novel SRY mutation leads to asymmetric SOX9 activation and is responsible for mixed 46,XY gonadal dysgenesis.
Klee P; Béna F; Birraux J; Dahoun S; Dirlewanger M; Girardin C; Plotton I; Rougemont AL; Morel Y; Schwitzgebel VM
Horm Res Paediatr; 2012; 78(3):188-92. PubMed ID: 22441105
[TBL] [Abstract][Full Text] [Related]
48. Embryonic testicular regression sequence: a part of the clinical spectrum of 46,XY gonadal dysgenesis.
Marcantonio SM; Fechner PY; Migeon CJ; Perlman EJ; Berkovitz GD
Am J Med Genet; 1994 Jan; 49(1):1-5. PubMed ID: 8172233
[TBL] [Abstract][Full Text] [Related]
49. DMRT gene cluster analysis in the platypus: new insights into genomic organization and regulatory regions.
El-Mogharbel N; Wakefield M; Deakin JE; Tsend-Ayush E; Grützner F; Alsop A; Ezaz T; Marshall Graves JA
Genomics; 2007 Jan; 89(1):10-21. PubMed ID: 16962738
[TBL] [Abstract][Full Text] [Related]
50. Coexistence of Trisomy 13 and SRY (-) XX Ovotesticular Disorder of Sex Development.
Ürel Demir G; Doğan ÖA; Şimşek Kiper PÖ; Utine GE; Boduroğlu K; Gucer S; Alikaşifoğlu M
Fetal Pediatr Pathol; 2017 Dec; 36(6):445-451. PubMed ID: 29220612
[TBL] [Abstract][Full Text] [Related]
51. OVOTESTICULAR DISORDER OF SEX DEVELOPMENT: A SINGLE-CENTER EXPERIENCE.
Khadilkar KS; Budyal SR; Kasaliwal R; Sathe PA; Kandalkar B; Sanghvi BV; Parelkar SV; Lila AR; Bandgar T; Shah NS
Endocr Pract; 2015 Jul; 21(7):770-6. PubMed ID: 25786559
[TBL] [Abstract][Full Text] [Related]
52. Array-CGH analysis in patients with syndromic and non-syndromic XY gonadal dysgenesis: evaluation of array CGH as diagnostic tool and search for new candidate loci.
Ledig S; Hiort O; Scherer G; Hoffmann M; Wolff G; Morlot S; Kuechler A; Wieacker P
Hum Reprod; 2010 Oct; 25(10):2637-46. PubMed ID: 20685758
[TBL] [Abstract][Full Text] [Related]
53. 46 XY Ovotesticular Disorder: A Rare Case Report with Review of Literature.
Meenal B; Meenakshi G; Pratibha S; Garima Y; Priyanka K; Poonam E
Gynecol Minim Invasive Ther; 2021; 10(3):171-173. PubMed ID: 34485063
[TBL] [Abstract][Full Text] [Related]
54. [A Case of 46,XY pure gonadal dysgenesis with loss of the sex-determining region of Y chromosome].
Yoon KH; Lee YJ
Korean J Lab Med; 2008 Apr; 28(2):151-4. PubMed ID: 18458512
[TBL] [Abstract][Full Text] [Related]
55. Long-term outcome of ovotesticular disorder of sex development: a single center experience.
Matsui F; Shimada K; Matsumoto F; Itesako T; Nara K; Ida S; Nakayama M
Int J Urol; 2011 Mar; 18(3):231-6. PubMed ID: 21255100
[TBL] [Abstract][Full Text] [Related]
56. Disorders of gonadal development: a broad clinical, cytogenetic and histopathologic spectrum.
Siklar Z; Berberoğlu M; Adiyaman P; Salih M; Tükün A; Cetinkaya E; Aycan Z; Evliyaoğlu O; Ergur AT; Oçal G
Pediatr Endocrinol Rev; 2007 Mar; 4(3):210-7. PubMed ID: 17551482
[TBL] [Abstract][Full Text] [Related]
57. Mixed Gonadal Dysgenesis with an unusual "inverted" Y chromosome.
Makhija D; Shah H; Tiwari C; Jayaswal S; Desale J
Dev Period Med; 2016; 20(3):178-180. PubMed ID: 27941186
[TBL] [Abstract][Full Text] [Related]
58. [XY type gonadal dysgenesis, trisomy X and variants].
Kikuchi I; Takeuchi H; Kinoshita K
Nihon Rinsho; 2004 Feb; 62(2):309-12. PubMed ID: 14968537
[TBL] [Abstract][Full Text] [Related]
59. 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]
60. [Study of sex determination gene (SRY) in 46,XY gonadal dysgenesis].
Boucekkine C; Vilain E; McElreavey K; Jaubert F; Brauner R; Thibaud E; Battin J; Toublanc JE; Kucheria K; Chaabouni S
Ann Endocrinol (Paris); 1994; 54(5):315-21. PubMed ID: 8085778
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]