136 related articles for article (PubMed ID: 9098487)
1. Telomeric fusion and chromosome instability in multiple tissues of a patient with mosaic Ullrich-Turner syndrome.
Sawyer JR; Swanson CM; Lukacs JL; Hassed SJ; Curtis MA; North PE; Kozlowski KJ; Pihoker C
Am J Med Genet; 1997 Apr; 69(4):383-7. PubMed ID: 9098487
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. X microchromosome with additional chromosome anomalies found in Ullrich-Turner syndrome.
Wydner KL; Li M; Singer-Granick C; Sciorra LJ; Krueger LJ
Am J Med Genet; 1995 Mar; 56(2):141-6. PubMed ID: 7625435
[TBL] [Abstract][Full Text] [Related]
4. [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]
5. Gonadoblastoma in patients with Ullrich-Turner syndrome.
Zelaya G; López Marti JM; Marino R; Garcia de Dávila MT; Gallego MS
Pediatr Dev Pathol; 2015; 18(2):117-21. PubMed ID: 25535833
[TBL] [Abstract][Full Text] [Related]
6. Histologic analysis of gonadal tissue in patients with Ullrich-Turner syndrome and derivative Y chromosomes.
Horn LC; Limbach A; Hoepffner W; Tröbs RB; Keller E; Froster UG; Richter CE; Jakubiczka S
Pediatr Dev Pathol; 2005; 8(2):197-203. PubMed ID: 15747103
[TBL] [Abstract][Full Text] [Related]
7. Gonadoblastoma in Turner syndrome patients with nonmosaic 45,X karyotype and Y chromosome sequences.
Canto P; Kofman-Alfaro S; Jiménez AL; Söderlund D; Barrón C; Reyes E; Méndez JP; Zenteno JC
Cancer Genet Cytogenet; 2004 Apr; 150(1):70-2. PubMed ID: 15041227
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Identification of the origin of ring/marker chromosomes in patients with Ullrich-Turner syndrome using X and Y specific alpha satellite DNA probes.
Tharapel SA; Wilroy RS; Keath AM; Rivas ML; Tharapel AT
Am J Med Genet; 1992 Mar; 42(5):720-3. PubMed ID: 1632446
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Novel karyotype in the Ullrich-Turner syndrome--45,X/46,X,r(X)/46,X, dic(X)--investigated with fluorescence in situ hybridization.
Robson L; Jackson J; Cowell C; Sillence D; Smith A
Am J Med Genet; 1994 Apr; 50(3):251-4. PubMed ID: 8042669
[TBL] [Abstract][Full Text] [Related]
13. Cytogenetic evaluation, fluorescence in situ hybridization, and molecular study of psu idic(X)(pter-->q22.3::q22.3-->pter) chromosome abberation in a girl with moderate growth retardation.
Petković I; Barisić I; Bago R
Croat Med J; 2003 Aug; 44(4):494-9. PubMed ID: 12950157
[TBL] [Abstract][Full Text] [Related]
14. Evidence for telomeric fusions as a mechanism for recurring structural aberrations of chromosome 11 in giant cell tumor of bone.
Sawyer JR; Goosen LS; Binz RL; Swanson CM; Nicholas RW
Cancer Genet Cytogenet; 2005 May; 159(1):32-6. PubMed ID: 15860354
[TBL] [Abstract][Full Text] [Related]
15. Double aneuploidy in three Egyptian patients: Down-Turner and Down-Klinefelter syndromes.
Zaki MS; Kamel AA; El-Ruby M
Genet Couns; 2005; 16(4):393-402. PubMed ID: 16440882
[TBL] [Abstract][Full Text] [Related]
16. PCR detection of Y-specific sequences in patients with Ullrich-Turner syndrome: clinical implications and limitations.
Osipova GR; Karmanov ME; Kozlova SI; Evgrafov OV
Am J Med Genet; 1998 Apr; 76(4):283-7. PubMed ID: 9545090
[TBL] [Abstract][Full Text] [Related]
17. PCR-based study of the presence of Y-chromosome sequences in patients with Ullrich-Turner syndrome.
Coto E; Toral JF; Menéndez MJ; Hernando I; Plasencia A; Benavides A; López-Larrea C
Am J Med Genet; 1995 Jul; 57(3):393-6. PubMed ID: 7677140
[TBL] [Abstract][Full Text] [Related]
18. Turner syndrome with pseudodicentric Y chromosome mosaicism.
Hsieh YY; Lin WC; Chang CC; Tsai FJ; Yu MT; Tsai HD; Tsai CH
J Assist Reprod Genet; 2002 Jun; 19(6):302-3. PubMed ID: 12166638
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. [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]
[Next] [New Search]