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22. 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]
23. United States survey on chromosome mosaicism and pseudomosaicism in prenatal diagnosis. Hsu LY; Perlis TE Prenat Diagn; 1984; 4 Spec No():97-130. PubMed ID: 6463035 [TBL] [Abstract][Full Text] [Related]
24. Mosaicism or pseudomosaicism: the problem of hypermodal cells in amniotic fluid cell culture. Zhang YJ; Garver KL; Marchese SG; Diggans GR; Muracca-Clemens M; Flecker D Prenat Diagn; 1984; 4(2):99-108. PubMed ID: 6739442 [TBL] [Abstract][Full Text] [Related]
25. Normal development in two six-year-old boys born after prenatal diagnosis of trisomy 20 mosaicism. Tolmie JL; Ferguson-Smith ME; Gilmore D; Ferguson-Smith MA Prenat Diagn; 1987 Oct; 7(8):597-601. PubMed ID: 3684964 [TBL] [Abstract][Full Text] [Related]
27. Mosaicism of 46,XX/47,XX,+9/47,XX,+?mar in the same amniotic fluid with apparent loss of one cell line after delivery. Herens C; Pierquin G; Verloes A; Schaaps JP; Frederic J Prenat Diagn; 1989 May; 9(5):373-5. PubMed ID: 2726702 [TBL] [Abstract][Full Text] [Related]
28. [Quick prenatal diagnosis using FISH in the analysis of non-cultured amniotic fluid cells]. Marguerat P; Gaide AC; Thonney F; Schorderet D Rev Med Suisse Romande; 2000 May; 120(5):401-7. PubMed ID: 10911743 [TBL] [Abstract][Full Text] [Related]
36. [Karyotype analysis of amniotic fluid cells and comparison of chromosomal abnormality rate during second trimester]. Zhang YP; Wu JP; Li XT; Lei CX; Xu JZ; Yin M Zhonghua Fu Chan Ke Za Zhi; 2011 Sep; 46(9):644-8. PubMed ID: 22176986 [TBL] [Abstract][Full Text] [Related]
37. Prenatal detection of chromosome aberrations after intercontinental transport of amniotic fluid. Gadow EC; Paz JE; Castilla EE; Rothe DJ; Cederqvist LL Int J Gynaecol Obstet; 1976; 14(2):164-70. PubMed ID: 10208 [No Abstract] [Full Text] [Related]
38. Prenatal diagnosis of an inherited translocation between chromosomes No. 9 and 18. Ebbin AJ; Wilson MG; Towner JW; Slaughter JP J Med Genet; 1973 Mar; 10(1):65-9. PubMed ID: 4697854 [TBL] [Abstract][Full Text] [Related]
39. Prenatal diagnosis of E trisomy syndrome by fetography. Ogita S; Hasegawa H; Matsumoto M; Kamei T; Shimamoto T Obstet Gynecol; 1974 Jun; 43(6):887-92. PubMed ID: 4597791 [No Abstract] [Full Text] [Related]
40. Prenatal diagnosis and clinical features of an individual with tetrasomy 18p and trisomy 18q mosaicism. Habecker-Green JG; Naeem R; Gold H; O'Grady JP; Kanaan C; Bayer-Zwirello L; Murray MS; Cohn GM J Perinatol; 1998; 18(5):395-8. PubMed ID: 9766419 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]