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459 related items for PubMed ID: 16810710
21. 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 [Abstract] [Full Text] [Related]
28. Issues arising from the prenatal diagnosis of some rare trisomy mosaics--the importance of cryptic fetal mosaicism. Daniel A, Wu Z, Darmanian A, Malafiej P, Tembe V, Peters G, Kennedy C, Adès L. Prenat Diagn; 2004 Jul; 24(7):524-36. PubMed ID: 15300743 [Abstract] [Full Text] [Related]
30. Origin of amnion and implications for evaluation of the fetal genotype in cases of mosaicism. Robinson WP, McFadden DE, Barrett IJ, Kuchinka B, Peñaherrera MS, Bruyère H, Best RG, Pedreira DA, Langlois S, Kalousek DK. Prenat Diagn; 2002 Dec; 22(12):1076-85. PubMed ID: 12454962 [Abstract] [Full Text] [Related]
31. Detection of mosaicism for primary trisomies in prenatal samples by QF-PCR and karyotype analysis. Donaghue C, Mann K, Docherty Z, Ogilvie CM. Prenat Diagn; 2005 Jan; 25(1):65-72. PubMed ID: 15662691 [Abstract] [Full Text] [Related]
35. 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 Jan; 53(4):197-200. PubMed ID: 20350623 [Abstract] [Full Text] [Related]