460 related articles for article (PubMed ID: 9793985)
1. Low-level mosaicism for both trisomy 15 and monosomy-X in amniotic fluid cells confirmed in fetal tissues.
Hansson K; Poelma WM; Zondervan HA; Leschot NJ
Prenat Diagn; 1998 Sep; 18(9):975-8. PubMed ID: 9793985
[TBL] [Abstract][Full Text] [Related]
2. Trisomy 12/monosomy X/normal female mosaicism: prenatal detection and confirmation in a liveborn.
Spiro R; Rita D; Jazmines L; Jones C; Booth CW
Prenat Diagn; 1996 Aug; 16(8):734-40. PubMed ID: 8878284
[TBL] [Abstract][Full Text] [Related]
3. Cytogenetic and molecular genetic characterization of trisomy 20 mosaicism in fetal blood and tissues.
Micale MA; Wolff DJ; Dickerman LH; Redline R; Conroy JM; Schwartz S
Prenat Diagn; 1996 Oct; 16(10):893-7. PubMed ID: 8938057
[TBL] [Abstract][Full Text] [Related]
4. Prenatal diagnosis of trisomy 3 mosaicism.
Zaslav AL; Pierno G; Davis J; Fougner A; Jacob J; Kazi R; Blumenthal D; Sturim S; Shaham M; Fox J
Prenat Diagn; 2004 Sep; 24(9):693-6. PubMed ID: 15386452
[TBL] [Abstract][Full Text] [Related]
5. Complete karyotype discrepancy between placental and fetal cells in a case of ring chromosome 18.
Fischer W; Dermitzel A; Osmers R; Pruggmayer M
Prenat Diagn; 2001 Jun; 21(6):481-3. PubMed ID: 11438954
[TBL] [Abstract][Full Text] [Related]
6. Clinical, cytogenetic, and molecular findings in 45,X/47,XX,+18 mosaicism: clinical report and review of the literature.
Schubert R; Eggermann T; Hofstaetter C; von Netzer B; Knöpfle G; Schwanitz G
Am J Med Genet; 2002 Jul; 110(3):278-82. PubMed ID: 12116238
[TBL] [Abstract][Full Text] [Related]
7. Chromosome mosaicism in 6,000 amniocenteses.
Wilson MG; Lin MS; Fujimoto A; Herbert W; Kaplan FM
Am J Med Genet; 1989 Apr; 32(4):506-13. PubMed ID: 2773995
[TBL] [Abstract][Full Text] [Related]
8. Amniotic trisomy 11 mosaicism--is it a benign finding?
Basel-Vanagaite L; Davidov B; Friedman J; Yeshaya Y; Magal N; Drasinover V; Shohat M
Prenat Diagn; 2006 Sep; 26(9):778-81. PubMed ID: 16810710
[TBL] [Abstract][Full Text] [Related]
9. Prenatal confirmation of true fetal trisomy 22 mosaicism by fetal skin biopsy following normal fetal blood sampling.
Berghella V; Wapner RJ; Yang-Feng T; Mahoney MJ
Prenat Diagn; 1998 Apr; 18(4):384-9. PubMed ID: 9602487
[TBL] [Abstract][Full Text] [Related]
10. Prenatally detected trisomy 4 and 6 mosaicism--cytogenetic results and clinical phenotype.
Wieczorek D; Prott EC; Robinson WP; Passarge E; Gillessen-Kaesbach G
Prenat Diagn; 2003 Feb; 23(2):128-33. PubMed ID: 12575019
[TBL] [Abstract][Full Text] [Related]
11. Prenatally detected trisomy 7 mosaicism in a dysmorphic child.
Kivirikko S; Salonen R; Salo A; von Koskull H
Prenat Diagn; 2002 Jul; 22(7):541-4. PubMed ID: 12124684
[TBL] [Abstract][Full Text] [Related]
12. Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13, 18, 20 and 21: karyotype-phenotype correlations.
Wallerstein R; Yu MT; Neu RL; Benn P; Lee Bowen C; Crandall B; Disteche C; Donahue R; Harrison B; Hershey D; Higgins RR; Jenkins LS; Jackson-Cook C; Keitges E; Khodr G; Lin CC; Luthardt FW; Meisner L; Mengden G; Patil SR; Rodriguez M; Sciorra LJ; Shaffer LG; Stetten G; Van Dyke DL; Wang H
Prenat Diagn; 2000 Feb; 20(2):103-22. PubMed ID: 10694683
[TBL] [Abstract][Full Text] [Related]
13. Prenatal diagnosis of mosaicism identified in amniotic fluid cell cultures.
Sahin FI; Yilmaz Z; Uckuyu A; Ozalp O; Tarim E; Deren O; Yanik F
Genet Couns; 2006; 17(3):341-8. PubMed ID: 17100203
[TBL] [Abstract][Full Text] [Related]
14. Non-mosaic trisomy 20 of paternal origin in chorionic villus and amniotic fluid also detected in fetal blood and other tissues.
Morales C; Cuatrecasas E; Mademont-Soler I; Clusellas N; Peruga E; Català V; Garrido C; Milà M; Soler A; Sánchez A
Eur J Med Genet; 2010; 53(4):197-200. PubMed ID: 20350623
[TBL] [Abstract][Full Text] [Related]
15. Pre- and postnatal diagnosis of trisomy 4 mosaicism.
Marion JP; Fernhoff PM; Korotkin J; Priest JH
Am J Med Genet; 1990 Nov; 37(3):362-5. PubMed ID: 2260566
[TBL] [Abstract][Full Text] [Related]
16. Trisomy 20 mosaicism and nonmosaic trisomy 20: a report of 2 cases.
Joó JG; Beke A; Tóth-Pál E; Hargitai B; Szigeti Z; Papp C; Papp Z
J Reprod Med; 2006 Mar; 51(3):209-12. PubMed ID: 16674019
[TBL] [Abstract][Full Text] [Related]
17. Mosaic trisomy 17 in amniocytes: phenotypic outcome, tissue distribution, and uniparental disomy studies.
Genuardi M; Tozzi C; Pomponi MG; Stagni ML; Della Monica M; Scarano G; Calvieri F; Torrisi L; Neri G
Eur J Hum Genet; 1999; 7(4):421-6. PubMed ID: 10352932
[TBL] [Abstract][Full Text] [Related]
18. Prenatal diagnosis of Prader-Willi syndrome using PW71 methylation analysis--uniparental disomy and the significance of residual trisomy 15.
Slater HR; Vaux C; Pertile M; Burgess T; Petrovic V
Prenat Diagn; 1997 Feb; 17(2):109-13. PubMed ID: 9061757
[TBL] [Abstract][Full Text] [Related]
19. Prenatal diagnosis of an infant with mosaic trisomy 16 of paternal origin.
Paulyson KJ; Sherer DM; Christian SL; Lewis KM; Ledbetter DH; Salafia CM; Meck JM
Prenat Diagn; 1996 Nov; 16(11):1021-6. PubMed ID: 8953635
[TBL] [Abstract][Full Text] [Related]
20. Trisomy 7 mosaicism at amniocentesis: interphase FISH, QF-PCR, and aCGH analyses on uncultured amniocytes for rapid distinguishing of true mosaicism from pseudomosaicism.
Chen CP; Huang HK; Su YN; Chern SR; Su JW; Lee CC; Town DD; Chen WL; Chen YT; Wang W
Taiwan J Obstet Gynecol; 2012 Mar; 51(1):77-82. PubMed ID: 22482973
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]