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14. Parental mosaic trisomy 21 detected following maternal cell contamination of an amniotic fluid specimen from a normal male pregnancy. Street ML; Barber JC; Boyle TA; Ellis KH; Bullman H; Homfray T Prenat Diagn; 2007 Sep; 27(9):858-60. PubMed ID: 17554802 [TBL] [Abstract][Full Text] [Related]
15. Follow-up of infants with amniotic fluid trisomy 20 mosaicism. Abuelo DN; Barsel-Bowers G; Zartler AS Am J Med Genet; 1986 Jul; 24(3):475-81. PubMed ID: 3728566 [TBL] [Abstract][Full Text] [Related]
16. Trisomy 12 mosaicism in amniocytes and dysmorphic child despite normal chromosomes in fetal blood sample. von Koskull H; Ritvanen A; Ammälä P; Gahmberg N; Salonen R Prenat Diagn; 1989 Jun; 9(6):433-7. PubMed ID: 2762235 [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. Trisomy 5 mosaicism in amniotic fluid with normal outcome. Casamassima AC; Wilmot PL; Mahoney MJ; Scott RV; Shapiro LR Clin Genet; 1989 Apr; 35(4):282-4. PubMed ID: 2714015 [TBL] [Abstract][Full Text] [Related]
19. Confirmation of true mosaic trisomy 20 in a phenotypically normal liveborn male. Brothman AR; Rehberg K; Storto PD; Phillips SE; Mosby RT Clin Genet; 1992 Jul; 42(1):47-9. PubMed ID: 1516227 [TBL] [Abstract][Full Text] [Related]
20. Multiple congenital anomalies in a child born after prenatal diagnosis of trisomy 20 mosaicism. Holzgreve W; Golabi M; Bradley J Clin Genet; 1986 Apr; 29(4):342-4. PubMed ID: 2424648 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]