These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
170 related articles for article (PubMed ID: 30678103)
41. Chromosomal abnormalities not currently detected by cell-free fetal DNA: a retrospective analysis at a single center. Shani H; Goldwaser T; Keating J; Klugman S Am J Obstet Gynecol; 2016 Jun; 214(6):729.e1-729.e11. PubMed ID: 26721783 [TBL] [Abstract][Full Text] [Related]
42. [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]
43. Rapid prenatal diagnosis of aneuploidies in uncultured amniocytes by fluorescence in situ hybridization. Evaluation of >3,000 cases. Eiben B; Trawicki W; Hammans W; Goebel R; Pruggmayer M; Epplen JT Fetal Diagn Ther; 1999; 14(4):193-7. PubMed ID: 10420039 [TBL] [Abstract][Full Text] [Related]
44. Molecular cytogenetic analysis of term placentae suspected of mosaicism using fluorescence in situ hybridization. Schuring-Blom GH; Keijzer M; Jakobs ME; Van den Brande DM; Visser HM; Wiegant J; Hoovers JM; Leschot NJ Prenat Diagn; 1993 Aug; 13(8):671-9. PubMed ID: 8284286 [TBL] [Abstract][Full Text] [Related]
45. Fluorescence in situ hybridization in uncultured amniocytes for detection of aneuploidy in 4210 prenatal cases. Jia CW; Wang SY; Ma YM; Lan YL; Si YM; Yu L; Zhou LY Chin Med J (Engl); 2011 Apr; 124(8):1164-8. PubMed ID: 21542989 [TBL] [Abstract][Full Text] [Related]
46. Prenatal diagnosis of a distal 3p deletion associated with fetoplacental chromosomal discrepancy and confined placental mosaicism detected by array comparative genomic hybridization. Chen CP; Chen YY; Chern SR; Wu PS; Su JW; Chen WL; Wang W Taiwan J Obstet Gynecol; 2013 Jun; 52(2):278-84. PubMed ID: 23915866 [TBL] [Abstract][Full Text] [Related]
47. Detection of no isochromosome 20q by interphase fluorescent in situ hybridization on uncultured amniocytes in a pregnancy with mosaic isochromosome 20q in cultured amniocytes at amniocentesis. Chen CP; Su JW; Chern SR; Kuo YL; Wu PS; Lee MS; Yang CW; Wang W Taiwan J Obstet Gynecol; 2015 Feb; 54(1):58-61. PubMed ID: 25675921 [TBL] [Abstract][Full Text] [Related]
48. [A preliminary study on the application of array comparative genomic hybridization for preimplantaion genetic diagnosis]. Xie Y; Xu Y; Miao B; Zeng Y; Zhou C Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Jun; 30(3):283-7. PubMed ID: 23744315 [TBL] [Abstract][Full Text] [Related]
49. [Clinical value of genome-wide high resolution chromosomal microarray analysis in etiological study of fetuses with congenital heart defects]. Wu X; Fu F; Li R; Pan M; Han J; Zhen L; Yang X; Zhang Y; Li F; Liao C Zhonghua Fu Chan Ke Za Zhi; 2014 Dec; 49(12):893-8. PubMed ID: 25608988 [TBL] [Abstract][Full Text] [Related]
50. Confined placental mosaicism and its impact on confirmation of NIPT results. Mardy A; Wapner RJ Am J Med Genet C Semin Med Genet; 2016 Jun; 172(2):118-22. PubMed ID: 27184347 [TBL] [Abstract][Full Text] [Related]
51. Mosaic trisomy 15 at amniocentesis: Prenatal diagnosis, molecular genetic analysis and literature review. Chen CP; Chern SR; Chen YN; Wu PS; Yang CW; Chen LF; Wang W Taiwan J Obstet Gynecol; 2015 Aug; 54(4):426-31. PubMed ID: 26384064 [TBL] [Abstract][Full Text] [Related]
52. Prenatal cytogenetic abnormalities: correlations of structural rearrangements and ultrasonographically detected fetal anomalies. Hume RF; Kilmer-Ernst P; Wolfe HM; Ebrahim SA; Treadwell MC; Johnson MP; Evans MI Am J Obstet Gynecol; 1995 Oct; 173(4):1334-6. PubMed ID: 7485349 [TBL] [Abstract][Full Text] [Related]
53. A rare de novo duplication of chromosome 21q22.12 → q22.3 with other concomitant deletion and duplication of small fragments in 21q associated with Down syndrome: Prenatal diagnosis, molecular cytogenetic characterization. Qi Q; Zhou X; Jiang Y; Hao N; Zhou J; Zhang L Mol Cytogenet; 2013 Mar; 6(1):11. PubMed ID: 23497671 [TBL] [Abstract][Full Text] [Related]
54. Application of non-invasive prenatal testing in late gestation in a pregnancy associated with intrauterine growth restriction and trisomy 22 confined placental mosaicism. Chen CP; Tsai C; Lin MH; Chern SR; Chen SW; Lai ST; Chen WL; Pan CW; Wang W Taiwan J Obstet Gynecol; 2017 Oct; 56(5):691-693. PubMed ID: 29037560 [TBL] [Abstract][Full Text] [Related]
55. A pregnancy with discordant fetal and placental chromosome 18 aneuploidies revealed by invasive and noninvasive prenatal diagnosis. Chen C; Cram DS; Xie F; Wang P; Xu X; Li H; Song Z; Chen D; Zhang J; Tang S Reprod Biomed Online; 2014 Jul; 29(1):136-9. PubMed ID: 24797099 [TBL] [Abstract][Full Text] [Related]
56. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 3. Chen CP; Ko TM; Chen CY; Chern SR; Wu PS; Chen SW; Wu FT; Pan CW; Wang W Taiwan J Obstet Gynecol; 2019 Nov; 58(6):864-868. PubMed ID: 31759544 [TBL] [Abstract][Full Text] [Related]