392 related articles for article (PubMed ID: 11693789)
1. Different chromosome Y abnormalities in Turner syndrome.
Bağci G; Acar H; Tomruk H
Genet Couns; 2001; 12(3):255-61. PubMed ID: 11693789
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. [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]
4. Cytogenetic and molecular investigations of Y chromosome sequences and their role in Turner syndrome.
Quilter CR; Taylor K; Conway GS; Nathwani N; Delhanty JD
Ann Hum Genet; 1998 Mar; 62(Pt 2):99-106. PubMed ID: 9759471
[TBL] [Abstract][Full Text] [Related]
5. Phenotype/karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases.
Hsu LY
Am J Med Genet; 1994 Nov; 53(2):108-40. PubMed ID: 7856637
[TBL] [Abstract][Full Text] [Related]
6. [Identification of sex chromosome markers using fluorescence in situ hybridization (FISH)].
González-del-Angel A; Blanco B; del Castillo V; Carnevale A
Rev Invest Clin; 1995; 47(2):117-25. PubMed ID: 7610280
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. [Diagnosis of sex chromosome abnormality by fluorescence in-situ hybridization].
Huang Y; Sun X; Li Q
Zhonghua Yi Xue Za Zhi; 1999 Feb; 79(2):106-8. PubMed ID: 11601014
[TBL] [Abstract][Full Text] [Related]
9. [Use of molecular cytogenetic techniques for establishing the origin of chromosome markers in patients with Turner phenotype].
Bocian E; Stańczak H; Wiśniewski A; Mazurczak T; Stankiewicz P
Pediatr Pol; 1996 Mar; 71(3):203-9. PubMed ID: 8966091
[TBL] [Abstract][Full Text] [Related]
10. [45,X/46,X,del(Yq) sex chromosome mosaicism--analysis of the phenotypic expression].
Werner W; John B; Tuschy U; Knorr B; Herrmann FH
Zentralbl Gynakol; 1985; 107(5):265-79. PubMed ID: 3993267
[TBL] [Abstract][Full Text] [Related]
11. Paternally derived der(7)t(Y;7)(p11.1 approximately 11.2;p22.3)dn in a mosaic case with Turner syndrome.
Polityko AD; Khurs OM; Kulpanovich AI; Mosse KA; Solntsava AV; Rumyantseva NV; Naumchik IV; Liehr T; Weise A; Mkrtchyan H
Eur J Med Genet; 2009; 52(4):207-10. PubMed ID: 19375526
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. [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]
14. Determining the origins and the structural aberrations of small marker chromosomes in two cases of 45,X/46,X, + mar by use of chromosome-specific DNA probes.
Lin CC; Meyne J; Sasi R; Bowen P; Unger T; Tainaka T; Hadro TA; Hoo JJ
Am J Med Genet; 1990 Sep; 37(1):71-8. PubMed ID: 2240047
[TBL] [Abstract][Full Text] [Related]
15. Identification of Y-chromosomal DNA in a Turner syndrome mosaic by polymerase chain reaction.
Louie E; Nemeti M; Torfi H; Poskanzer LB; Anderson FR; Johnson JP
Ann Genet; 1991; 34(3-4):252-5. PubMed ID: 1809235
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. [Marker chromosome analysis in Chinese patients with Turner syndrome by fluorescence in situ hybridization].
Liang Y; Luo XP
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug; 22(4):435-7. PubMed ID: 16086285
[TBL] [Abstract][Full Text] [Related]
18. Evaluation of sex chromosome aneuploidies in women with Turner's syndrome by G-banding and FISH. A serial case study.
Cortés-Gutiérrez EI; Cerda-Flores RM; Silva-Cudish JB; Dávila-Rodríguez MI; Hernández-Herrera R; Leal-Garza CH
J Reprod Med; 2003 Oct; 48(10):804-8. PubMed ID: 14628733
[TBL] [Abstract][Full Text] [Related]
19. A variant Klinefelter syndrome patient with an XXY/XX/XY karyotype studied by GTG-banding and fluorescence in situ hybridization.
Mark HF; Bai H; Sotomayor E; Mark S; Zolnierz K; Airall E; Sigman M
Exp Mol Pathol; 1999 Sep; 67(1):50-6. PubMed ID: 10493892
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
