181 related articles for article (PubMed ID: 25200913)
1. Bladder exstrophy-epispadias complex and triple-X syndrome: incidental finding or causality?
Ramaekers P; Loeys B; von Lowtzow C; Reutter H; Leroy Y; Colpaert C; Blaumeiser B; Janssens K; Parizel M; Jacquemyn Y
Birth Defects Res A Clin Mol Teratol; 2014 Oct; 100(10):797-800. PubMed ID: 25200913
[TBL] [Abstract][Full Text] [Related]
2. Fetal axillary cystic hygroma: a novel association with triple X syndrome.
Iskender C; Tarım E; Cok T; Yalcinkaya C; Kalaycı H; Sahin F
Birth Defects Res A Clin Mol Teratol; 2012 Nov; 94(11):955-7. PubMed ID: 23109196
[TBL] [Abstract][Full Text] [Related]
3. Undetected sex chromosome aneuploidy by chromosomal microarray.
Markus-Bustani K; Yaron Y; Goldstein M; Orr-Urtreger A; Ben-Shachar S
Prenat Diagn; 2012 Nov; 32(11):1117-8. PubMed ID: 23034780
[TBL] [Abstract][Full Text] [Related]
4. A finding in genetic polymorphism analysis study: A case of non-mosaic 47, XXX without manifestations.
Yang X; Ye Z; Zhang X; Wang H; Liu C
Leg Med (Tokyo); 2017 Jul; 27():38-42. PubMed ID: 28697408
[TBL] [Abstract][Full Text] [Related]
5. Clinical and molecular characterization of the bladder exstrophy-epispadias complex: analysis of 232 families.
Boyadjiev SA; Dodson JL; Radford CL; Ashrafi GH; Beaty TH; Mathews RI; Broman KW; Gearhart JP
BJU Int; 2004 Dec; 94(9):1337-43. PubMed ID: 15610117
[TBL] [Abstract][Full Text] [Related]
6. Genome-wide analysis for micro-aberrations in familial exstrophy of the bladder using array-based comparative genomic hybridization.
Reutter H; Hoischen A; Ludwig M; Stein R; Radlwimmer B; Engels H; Wolffenbuttel KP; Weber RG
BJU Int; 2007 Sep; 100(3):646-50. PubMed ID: 17669146
[TBL] [Abstract][Full Text] [Related]
7. A rare case of NIPT discrepancy caused by the placental mosaicism of three different karyotypes, 47,XXX, 47,XX,+21, and 48,XXX,+21.
Li J; Xie M; Wang F; Ma J; Li J; Chen C; Li Z; Wang J; Zhang Y; Li Y
Mol Genet Genomic Med; 2020 Aug; 8(8):e1279. PubMed ID: 32463164
[TBL] [Abstract][Full Text] [Related]
8. Rare case of massive congenital bilateral chylothorax in a hydropic fetus with true mosaicism 47,XXX/46,XX.
Cremonini G; Poggi A; Capucci R; Vesce F; Patella A; Marci R
J Obstet Gynaecol Res; 2014 Jan; 40(1):259-62. PubMed ID: 23937348
[TBL] [Abstract][Full Text] [Related]
9. Expanding the phenotype of Triple X syndrome: A comparison of prenatal versus postnatal diagnosis.
Wigby K; D'Epagnier C; Howell S; Reicks A; Wilson R; Cordeiro L; Tartaglia N
Am J Med Genet A; 2016 Nov; 170(11):2870-2881. PubMed ID: 27644018
[TBL] [Abstract][Full Text] [Related]
10. Y chromosome aberration in a patient with cloacal-bladder exstrophy-epispadias complex: an unusual finding.
Nishi MY; Martins TC; Costa EM; Mendonca BB; Giron AM; Domenice S
Arq Bras Endocrinol Metabol; 2013 Mar; 57(2):148-52. PubMed ID: 23525294
[TBL] [Abstract][Full Text] [Related]
11. Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical region.
Draaken M; Baudisch F; Timmermann B; Kuhl H; Kerick M; Proske J; Wittler L; Pennimpede T; Ebert AK; Rösch W; Stein R; Bartels E; von Lowtzow C; Boemers TM; Herms S; Gearhart JP; Lakshmanan Y; Kockum CC; Holmdahl G; Läckgren G; Nordenskjöld A; Boyadjiev SA; Herrmann BG; Nöthen MM; Ludwig M; Reutter H
Birth Defects Res A Clin Mol Teratol; 2014 Jun; 100(6):512-7. PubMed ID: 24764164
[TBL] [Abstract][Full Text] [Related]
12. Triple X syndrome.
Afshan A
J Pak Med Assoc; 2012 Apr; 62(4):392-4. PubMed ID: 22755288
[TBL] [Abstract][Full Text] [Related]
13. Bladder exstrophy and epispadias complex in sibling: case report and review of literature.
Kajbafzadeh AM; Tajik P; Payabvash S; Farzan S; Solhpour AR
Pediatr Surg Int; 2006 Sep; 22(9):767-70. PubMed ID: 16896811
[TBL] [Abstract][Full Text] [Related]
14. Register based study of bladder exstrophy-epispadias complex: prevalence, associated anomalies, prenatal diagnosis and survival.
Jayachandran D; Bythell M; Platt MW; Rankin J
J Urol; 2011 Nov; 186(5):2056-60. PubMed ID: 21944104
[TBL] [Abstract][Full Text] [Related]
15. [Double aneuploidy (trisomy X, trisomy 18) in a newborn with trisomy 18 phenotype].
Pachajoa H
Arch Argent Pediatr; 2013; 111(4):e101-4. PubMed ID: 23912296
[TBL] [Abstract][Full Text] [Related]
16. Epidemiological survey of 214 families with bladder exstrophy-epispadias complex.
Gambhir L; Höller T; Müller M; Schott G; Vogt H; Detlefsen B; Ebert AK; Fisch M; Beaudoin S; Stein R; Boyadjiev SA; Gearhart JP; Rösch W; Utsch B; Boemers TM; Reutter H; Ludwig M
J Urol; 2008 Apr; 179(4):1539-43. PubMed ID: 18295266
[TBL] [Abstract][Full Text] [Related]
17. A case with bladder exstrophy and unbalanced X chromosome rearrangement.
Soderhall C; Lundin J; Lagerstedt-Robinson K; Grigelioniene G; Lackgren G; Kockum CC; Nordenskjold A
Eur J Pediatr Surg; 2014 Aug; 24(4):353-9. PubMed ID: 23801353
[TBL] [Abstract][Full Text] [Related]
18. The Genomic Architecture of Bladder Exstrophy Epispadias Complex.
Beaman GM; Cervellione RM; Keene D; Reutter H; Newman WG
Genes (Basel); 2021 Jul; 12(8):. PubMed ID: 34440323
[TBL] [Abstract][Full Text] [Related]
19. PLAGL1 epimutation and bladder exstrophy: Coincidence or concurrent etiology?
Kolarova J; Bens S; Ammerpohl O; Hilger AC; Zhang R; Reutter H; Siebert R
Birth Defects Res A Clin Mol Teratol; 2016 Aug; 106(8):724-8. PubMed ID: 27223093
[TBL] [Abstract][Full Text] [Related]
20. Only a minority of sex chromosome abnormalities are detected by a national prenatal screening program for Down syndrome.
Viuff MH; Stochholm K; Uldbjerg N; Nielsen BB; ; Gravholt CH
Hum Reprod; 2015 Oct; 30(10):2419-26. PubMed ID: 26251461
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
