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2. Postnatal confirmation of prenatally diagnosed trisomy 16 mosaicism in two phenotypically abnormal liveborns. Pletcher BA; Sanz MM; Schlessel JS; Kunaporn S; McKenna C; Bialer MG; Alonso ML; Zaslav AL; Brown WT; Ray JH Prenat Diagn; 1994 Oct; 14(10):933-40. PubMed ID: 7899268 [TBL] [Abstract][Full Text] [Related]
3. Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicism. Christian SL; Smith AC; Macha M; Black SH; Elder FF; Johnson JM; Resta RG; Surti U; Suslak L; Verp MS; Ledbetter DH Prenat Diagn; 1996 Apr; 16(4):323-32. PubMed ID: 8734806 [TBL] [Abstract][Full Text] [Related]
4. Prenatal diagnosis of mosaic tetrasomy 12p/trisomy 12p by fluorescent in situ hybridization in amniotic fluid cells: a case report of Pallister-Killian syndrome. Los FJ; Van Opstal D; Schol MP; Gaillard JL; Brandenburg H; Van Den Ouweland AM; in 't Veld PA Prenat Diagn; 1995 Dec; 15(12):1155-9. PubMed ID: 8750296 [TBL] [Abstract][Full Text] [Related]
5. Prenatal diagnosis of trisomy 9 mosaic presenting as a case of Dandy-Walker malformation. Bureau YA; Fraser W; Fouquet B Prenat Diagn; 1993 Feb; 13(2):79-85. PubMed ID: 8464839 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Tissue-specific mosaicism among fetuses with prenatally diagnosed diaphragmatic hernia. Donnenfeld AE; Campbell TJ; Byers J; Librizzi RJ; Weiner S Am J Obstet Gynecol; 1993 Oct; 169(4):1017-21. PubMed ID: 8238112 [TBL] [Abstract][Full Text] [Related]
8. Complex mosaicism associated with trisomy 9. Smoleniec JS; Davies T; Lunt P; Berry PJ; James D Prenat Diagn; 1993 Mar; 13(3):211-3. PubMed ID: 8506220 [TBL] [Abstract][Full Text] [Related]
10. Prenatal diagnosis of mosaic trisomy 9. Chen CP; Hung FY; Su YN; Chern SR; Su JW; Lee CC; Chen YT; Chen WL; Wang W Taiwan J Obstet Gynecol; 2011 Dec; 50(4):549-53. PubMed ID: 22212338 [No Abstract] [Full Text] [Related]
11. Mosaic trisomy 16 in a fetus: the complex relationship between phenotype and genetic mechanisms. Moradkhani K; Puechberty J; Blanchet P; Coubes C; Lallaoui H; Lewin P; Lefort G; Sarda P Prenat Diagn; 2006 Dec; 26(12):1179-82. PubMed ID: 17075795 [TBL] [Abstract][Full Text] [Related]
12. Mosaic deletion-duplication syndrome of chromosome 3: prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy. Chen CP; Su YN; Hsu CY; Chern SR; Lee CC; Chen YT; Chen WL; Wang W Taiwan J Obstet Gynecol; 2011 Dec; 50(4):485-91. PubMed ID: 22212322 [TBL] [Abstract][Full Text] [Related]
13. On the significance of true trisomy 20 mosaicism in amniotic fluid culture. Djalali M; Steinbach P; Schwinger E; Schwanitz G; Tettenborn U; Wolf M Hum Genet; 1985; 69(4):321-6. PubMed ID: 3988281 [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. The role of cordocentesis in assessment of mosaicism found in amniotic fluid cell culture. Shalev E; Zalel Y; Weiner E; Cohen H; Shneur Y Acta Obstet Gynecol Scand; 1994 Feb; 73(2):119-22. PubMed ID: 8116349 [TBL] [Abstract][Full Text] [Related]