483 related articles for article (PubMed ID: 16530711)
1. Isodicentric Y (p11.32) chromosome in an infant with mixed gonadal dysgenesis.
Aktas D; Alikasifoglu M; Gonc N; Senocak ME; Tuncbilek E
Eur J Med Genet; 2006; 49(2):141-9. PubMed ID: 16530711
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Characterization of an isodicentric Y-chromosome for the long arm in a newborn with mixed gonadal dysgenesis.
Kohn B; Kleyman SM; Conte RA; Macera MJ; Glassberg K; Verma RS
Ann Genet; 1997; 40(1):10-3. PubMed ID: 9150844
[TBL] [Abstract][Full Text] [Related]
4. Laparoscopic diagnosis and treatment of a phenotypic girl with mosaic 45,XO/46,X,idic(Y) mixed gonadal dysgenesis.
Mizuno K; Kojima Y; Kurokawa S; Mizuno H; Kohri K; Hayashi Y
J Pediatr Surg; 2009 Jan; 44(1):e1-3. PubMed ID: 19159702
[TBL] [Abstract][Full Text] [Related]
5. Cytogenetic and molecular characterization of two isodicentric Y chromosomes.
Stankiewicz P; Hélias-Rodzewicz Z; Jakubów-Durska K; Bocian E; Obersztyn E; Rappold GA; Mazurczak T
Am J Med Genet; 2001 Jun; 101(1):20-5. PubMed ID: 11343332
[TBL] [Abstract][Full Text] [Related]
6. Evidence of a mechanism for isodicentric chromosome Y formation in a 45,X/46,X,idic(Y)(p11.31)/46,X,del(Y)(p11.31) mosaic karyotype.
Reshmi SC; Miller JL; Deplewski D; Close C; Henderson LJ; Littlejohn E; Schwartz S; Waggoner DJ
Eur J Med Genet; 2011; 54(2):161-4. PubMed ID: 21078420
[TBL] [Abstract][Full Text] [Related]
7. Prenatal and postnatal characterization of Y chromosome structural anomalies by molecular cytogenetic analysis.
Hernando C; Carrera M; Ribas I; Parear N; Baraibar R; Egocue J; Fuster C
Prenat Diagn; 2002 Sep; 22(9):802-5. PubMed ID: 12224075
[TBL] [Abstract][Full Text] [Related]
8. Mix gonadal dysgenesis associated with ring Y chromosome mosaics in a phenotypic male.
Lopez-Valdes JA; Nieto K; Najera N; Cervantes A; Kofman-Alfaro S; Queipo G
Sex Dev; 2009; 3(4):177-82. PubMed ID: 19752596
[TBL] [Abstract][Full Text] [Related]
9. [Screening for Y chromosome sequences in patients with Turner syndrome].
Ferrão L; Lopes ML; Limbert C; Marques B; Boieiro F; Silva M; Marques R; Lavinha J; Mota A; Gonçalves J
Acta Med Port; 2002; 15(2):89-100. PubMed ID: 15524154
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. A Turner-like phenotype in a girl with an isodicentric fluorescent Y chromosome mosaicism.
Bergendi E; Plöchl E; Vlasak I; Rittinger O; Muss W
Klin Padiatr; 1997; 209(3):133-6. PubMed ID: 9183775
[TBL] [Abstract][Full Text] [Related]
12. Molecular analysis of an idic(Y)(qter -->p11.32::p11.32-->qter) chromosome from a female patient with a complex karyotype.
Fernandez R; Pasaro E
Genet Mol Res; 2006 Jun; 5(2):399-406. PubMed ID: 16819718
[TBL] [Abstract][Full Text] [Related]
13. Clinical and molecular cytogenetic studies in three infertile patients with mosaic rearranged Y chromosomes.
Bettio D; Venci A; Rizzi N; Negri L; Setti PL
Hum Reprod; 2006 Apr; 21(4):972-5. PubMed ID: 16484313
[TBL] [Abstract][Full Text] [Related]
14. Detection of Y chromosome sequences in a 45,X/46,XXq--patient by Southern blot analysis of PCR-amplified DNA and fluorescent in situ hybridization (FISH).
Kocova M; Siegel SF; Wenger SL; Lee PA; Nalesnik M; Trucco M
Am J Med Genet; 1995 Feb; 55(4):483-8. PubMed ID: 7762591
[TBL] [Abstract][Full Text] [Related]
15. [Y chromosome structural abnormalities and Turner's syndrome].
Ravel C; Siffroi JP
Gynecol Obstet Fertil; 2009 Jun; 37(6):511-8. PubMed ID: 19464936
[TBL] [Abstract][Full Text] [Related]
16. Mixed gonadal dysgenesis in a child with isodicentric Y chromosome: Does the relative proportion of the 45,X line really matter?
Shinawi M; Cain MP; Vanderbrink BA; Grignon DJ; Mensing D; Cooper ML; Bader P; Cheung SW
Am J Med Genet A; 2010 Jul; 152A(7):1832-7. PubMed ID: 20583182
[TBL] [Abstract][Full Text] [Related]
17. [Identification of the small supernumerary marker chromosomes in two patients with Turner syndrome].
Wen J; Liang D; Liao X; Xue J; Tang G; Xia Y; Long Z; Dai H; Wu L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Dec; 26(6):659-63. PubMed ID: 19953489
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. [Clinical, molecular and cytogenetic studies on 4 patients with 46, XX (SRY positive) male syndrome].
Xia XY; Cui YX; Lu HY; Yang B; Wang GH; Pan LJ; Hou BS; Ge YF; Shao Y; Yao B; Huang YF
Zhonghua Nan Ke Xue; 2007 Dec; 13(12):1094-7. PubMed ID: 18284058
[TBL] [Abstract][Full Text] [Related]
20. Screening for mutations in the SRY gene in patients with mixed gonadal dysgenesis or with Turner syndrome and Y mosaicism.
Canto P; Galicia N; Söderlund D; Escudero I; Méndez JP
Eur J Obstet Gynecol Reprod Biol; 2004 Jul; 115(1):55-8. PubMed ID: 15223166
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
