812 related articles for article (PubMed ID: 20445340)
21. Double mosaic aneuploidy: 45,X/47,XY,+8 in a male infant.
Schofield B; Babu A; Punales-Morejon D; Popescu S; Leiter E; Franklin B; Penchaszadeh VB
Am J Med Genet; 1992 Sep; 44(1):7-10. PubMed ID: 1519655
[TBL] [Abstract][Full Text] [Related]
22. Increased aneuploidy rates in spermatozoa of a male carrier of a trisomy 18 mosaicism.
Perrin A; Douet-Guilbert N; Le Bris MJ; May-Panloup P; Guichet A; Amice V; Amice J; De Braekeleer M; Morel F
Int J Androl; 2009 Jun; 32(3):231-4. PubMed ID: 18217987
[TBL] [Abstract][Full Text] [Related]
23. Mosaic double aneuploidy of X and G chromosomes.
Osborne RA; Hennigar GR; Barnett CD
Am J Ment Defic; 1975 May; 79(6):644-7. PubMed ID: 125038
[TBL] [Abstract][Full Text] [Related]
24. [Identification and characterization of marker chromosome in Turner syndrome].
Tan YQ; Cheng DH; DI YF; Li LY; Lu GX
Zhonghua Fu Chan Ke Za Zhi; 2007 Oct; 42(10):679-82. PubMed ID: 18241543
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. [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]
27. 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]
28. 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]
29. [Prenatal diagnosis of common chromosomal aneuploidies on uncultured amniotic fluid cells by fluorescence in situ hybridization].
Xiao HM; Tan YQ; Li LY; Lu GX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Dec; 21(6):608-10. PubMed ID: 15583993
[TBL] [Abstract][Full Text] [Related]
30. Mosaic trisomy 22: a case presentation and literature review of trisomy 22 phenotypes.
Crowe CA; Schwartz S; Black CJ; Jaswaney V
Am J Med Genet; 1997 Sep; 71(4):406-13. PubMed ID: 9286446
[TBL] [Abstract][Full Text] [Related]
31. [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]
32. A case of myelodysplastic syndrome with acquired monosomy 7 in a child with a constitutional t(1;19) and a mosaicism for trisomy 21.
Hu J; Shekhter-Levin S; Shaw PH; Bay C; Kochmar S; Surti U
Cancer Genet Cytogenet; 2005 Jan; 156(1):62-7. PubMed ID: 15588858
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. Early Bilateral Gonadoblastoma in a Young Child with Mosaicism for Turner Syndrome and Trisomy 18 with Y Chromosome.
MacMahon JM; O'Sullivan MJ; McDermott M; Quinn F; Morris T; Green AJ; Betts DR; O'Connell SM
Horm Res Paediatr; 2017; 87(2):130-135. PubMed ID: 27614983
[TBL] [Abstract][Full Text] [Related]
35. [Detection of aneuploidies using in situ hybridization in cells of the oral mucosa].
Frías S; Ordaz G; Blanco B; Molina B; del Castillo V; Carnevale A
Rev Invest Clin; 1996; 48(5):355-60. PubMed ID: 9005512
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. [Double aneuploidy: 46,XX-45,XO-47,XX,G+. Case report].
Grosse KP; Hopfengärtner F; Schwanitz G
Humangenetik; 1971; 13(4):333-7. PubMed ID: 4257570
[No Abstract] [Full Text] [Related]
38. 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]
39. Increasing role of cytogenetics in pediatric practice.
Dayakar S; Rani DS; Babu SJ; Srilatha K; Jayanthi U; Goud KI; Jain D; Raina V
Genet Test Mol Biomarkers; 2010 Apr; 14(2):197-204. PubMed ID: 20384456
[TBL] [Abstract][Full Text] [Related]
40. Molecular detection of cryptic Y-chromosomal material in patients with Turner syndrome.
Cortés-Gutiérrez EI; Herrera-Bartolo R; Dávila-Rodríguez MI; Palacios-Saucedo GC; Vargas-Villarreal J; Romero-Villarreal JB
Oncol Rep; 2012 Oct; 28(4):1205-10. PubMed ID: 22824904
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
