153 related articles for article (PubMed ID: 10748405)
21. Partial gonadal dysgenesis in a patient with a marker Y chromosome.
Fechner PY; Smith KD; Jabs EW; Migeon CJ; Berkovitz GD
Am J Med Genet; 1992 Apr; 42(6):807-12. PubMed ID: 1313209
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. Delineation of an isodicentric Y chromosome in a mosaic 45,X/46,X,idic(Y)(qter-p11.3::p11.3-qter) fetus by SRY sequencing, G-banding, FISH, SKY and study of distribution in different tissues.
Wu HH; Lee TH; Chen CD; Yeh KT; Chen M
J Formos Med Assoc; 2007 May; 106(5):403-10. PubMed ID: 17561477
[TBL] [Abstract][Full Text] [Related]
24. FISH analysis helps identify low-level mosaicism in Ullrich-Turner syndrome patients.
Wiktor A; Van Dyke DL
Genet Med; 2004; 6(3):132-5. PubMed ID: 15354330
[TBL] [Abstract][Full Text] [Related]
25. Supernumerary marker chromosomes (SMCs) in Turner syndrome are mostly derived from the Y chromosome.
Patsalis PC; Hadjimarcou MI; Velissariou V; Kitsiou-Tzeli S; Zera C; Syrrou M; Lyberatou E; Tsezou A; Galla A; Skordis N
Clin Genet; 1997 Mar; 51(3):184-90. PubMed ID: 9137884
[TBL] [Abstract][Full Text] [Related]
26. Discordant phenotypes and 45,X/46,X,idic(Y).
Kelly TE; Franko JB; Rogol A; Golden WL
J Med Genet; 1998 Oct; 35(10):862-4. PubMed ID: 9783714
[TBL] [Abstract][Full Text] [Related]
27. Turner's syndrome and chromosome Y.
Held KR
Lancet; 1993 Jul; 342(8864):128-9. PubMed ID: 8101248
[No Abstract] [Full Text] [Related]
28. 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]
29. Detection of low level sex chromosome mosaicism in Ullrich-Turner syndrome patients.
Wiktor AE; Van Dyke DL
Am J Med Genet A; 2005 Oct; 138A(3):259-61. PubMed ID: 16158437
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. 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]
32. Left-sided congenital heart lesions in mosaic Turner syndrome.
Bouayed Abdelmoula N; Abdelmoula B; Smaoui W; Trabelsi I; Louati R; Aloulou S; Aloulou W; Abid F; Kammoun S; Trigui K; Bedoui O; Denguir H; Mallek S; Ben Aziza M; Dammak J; Kaabi O; Abdellaoui N; Turki F; Kaabi A; Kamoun W; Jabeur J; Ltaif W; Chaker K; Fourati H; M'rabet S; Ben Ameur H; Gouia N; Mhiri MN; Rebai T
Mol Genet Genomics; 2018 Apr; 293(2):495-501. PubMed ID: 29196848
[TBL] [Abstract][Full Text] [Related]
33. A non-sex chromosome marker in a patient with an atypical Ullrich-Turner phenotype and mosaicism of 46,X,mar/46,XX.
Gray BA; Bent-Williams A; Wolff DJ; Zori RT
Clin Genet; 2001 Jul; 60(1):73-6. PubMed ID: 11531974
[TBL] [Abstract][Full Text] [Related]
34. Frequency of Y chromosomal material in Mexican patients with Ullrich-Turner syndrome.
López M; Canto P; Aguinaga M; Torres L; Cervantes A; Alfaro G; Méndez JP; Kofman-Alfaro S
Am J Med Genet; 1998 Mar; 76(2):120-4. PubMed ID: 9511973
[TBL] [Abstract][Full Text] [Related]
35. Analysis of the SRY gene in Turner syndrome patients with Y chromosomal material.
Yorifuji T; Muroi J; Mamada M; Uematsu A; Kawai M; Momoi T; Kaji M; Yamanaka C; Nakahata T
J Med Genet; 2001 Nov; 38(11):E41. PubMed ID: 11694555
[No Abstract] [Full Text] [Related]
36. 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]
37. 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]
38. [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]
39. Detailed analysis of an idic(Y)(q11.21) in a mosaic karyotype.
Al-Achkar W; Wafa A; Liehr T; Klein E; Moassass F
Mol Med Rep; 2012 Aug; 6(2):293-6. PubMed ID: 22664581
[TBL] [Abstract][Full Text] [Related]
40. Mosaic male fetus of Turner syndrome with partial chromosome Y: A case report.
Xue D; Cao DH; Mu K; Lv Y; Yang J
J Obstet Gynaecol Res; 2018 Jun; 44(6):1158-1162. PubMed ID: 29517175
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
