341 related articles for article (PubMed ID: 9557898)
1. Dilemma of trisomy 20 mosaicism detected prenatally: is it an innocent finding?
Reish O; Wolach B; Amiel A; Kedar I; Dolfin T; Fejgin M
Am J Med Genet; 1998 Apr; 77(1):72-5. PubMed ID: 9557898
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Clinical, cytogenetic, and molecular findings of prenatally diagnosed mosaic trisomy 4.
Chen CP; Chern SR; Lee CC; Chang TY; Wang W; Tzen CY
Prenat Diagn; 2004 Jan; 24(1):38-44. PubMed ID: 14755408
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. A phenotypically normal liveborn male after prenatal diagnosis of trisomy 20 mosaicism.
Von Beust G; Bartels I; Zoll B
Genet Couns; 2003; 14(1):67-74. PubMed ID: 12725591
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. Clinical outcome and follow-up of the first reported case of Russell-Silver syndrome with the unique combination of maternal uniparental heterodisomy 7 and mosaic trisomy 7.
Font-Montgomery E; Stone KM; Weaver DD; Vance GH; Das S; Thurston VC
Birth Defects Res A Clin Mol Teratol; 2005 Aug; 73(8):577-82. PubMed ID: 16007591
[TBL] [Abstract][Full Text] [Related]
9. Trisomy 13 mosaicism: study of serial cytogenetic changes in a case from early pregnancy to infancy.
Chen M; Yeh GP; Shih JC; Wang BT
Prenat Diagn; 2004 Feb; 24(2):137-43. PubMed ID: 14974123
[TBL] [Abstract][Full Text] [Related]
10. Postnatal follow-up of prenatally diagnosed trisomy 16 mosaicism.
Langlois S; Yong PJ; Yong SL; Barrett I; Kalousek DK; Miny P; Exeler R; Morris K; Robinson WP
Prenat Diagn; 2006 Jun; 26(6):548-58. PubMed ID: 16683298
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. A further case of confined placental mosaicism for trisomy 2 associated with adverse pregnancy outcome.
Roberts E; Dunlop J; Davis GS; Churchill D; Davison EV
Prenat Diagn; 2003 Jul; 23(7):564-5. PubMed ID: 12868084
[TBL] [Abstract][Full Text] [Related]
13. Prenatal diagnosis of trisomy 6 mosaicism.
Destree A; Fourneau C; Dugauquier C; Rombout S; Sartenaer D; Gillerot Y
Prenat Diagn; 2005 May; 25(5):354-7. PubMed ID: 15906424
[TBL] [Abstract][Full Text] [Related]
14. Transposition of great arteries in an infant born after prenatal diagnosis of trisomy 20 mosaicism.
Karaoguz MY; Pala E; Kula S; Karaer K; Kan D; Nas T; Tunaoglu S
Genet Couns; 2007; 18(4):437-43. PubMed ID: 18286825
[TBL] [Abstract][Full Text] [Related]
15. Maternal uniparental isodisomy 20 in a foetus with trisomy 20 mosaicism: clinical, cytogenetic and molecular analysis.
Velissariou V; Antoniadi T; Gyftodimou J; Bakou K; Grigoriadou M; Christopoulou S; Hatzipouliou A; Donoghue J; Karatzis P; Katsarou E; Petersen MB
Eur J Hum Genet; 2002 Nov; 10(11):694-8. PubMed ID: 12404100
[TBL] [Abstract][Full Text] [Related]
16. Discrepancies in cytogenetic results between amniocytes and postnatally obtained blood: trisomy 9 mosaicism.
Kosaki R; Hanai S; Kakishima H; Okada MA; Hayashi S; Ito Y; Takahashi T; Kosaki K; Okuyama T
Congenit Anom (Kyoto); 2006 Jun; 46(2):115-7. PubMed ID: 16732770
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Mosaic trisomy 12 at amniocentesis: prenatal diagnosis and molecular genetic analysis.
Chen CP; Su YN; Su JW; Chern SR; Chen YT; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2013 Mar; 52(1):97-105. PubMed ID: 23548227
[TBL] [Abstract][Full Text] [Related]
20. [Intrauterine growth retardation associated with a mosaic trisomy 20 limited to the placenta. A case report].
Lacoste-Jugnet N; Depret-Mosser S; Vinatier D; Savary D; Dufour P; Lefebvre-Maunoury C; Monnier JC
J Gynecol Obstet Biol Reprod (Paris); 1995; 24(6):606-9. PubMed ID: 8830080
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]