170 related articles for article (PubMed ID: 30678103)
21. Detection of cytogenomic abnormalities by OncoScan microarray assay for products of conception from formalin-fixed paraffin-embedded and fresh fetal tissues.
Wen J; Grommisch B; DiAdamo A; Chai H; Ng SME; Hui P; Bale A; Mak W; Wang G; Li P
Mol Cytogenet; 2021 Apr; 14(1):21. PubMed ID: 33810806
[TBL] [Abstract][Full Text] [Related]
22. The predictive value of findings of the common aneuploidies, trisomies 13, 18 and 21, and numerical sex chromosome abnormalities at CVS: experience from the ACC U.K. Collaborative Study. Association of Clinical Cytogeneticists Prenatal Diagnosis Working Party.
Smith K; Lowther G; Maher E; Hourihan T; Wilkinson T; Wolstenholme J
Prenat Diagn; 1999 Sep; 19(9):817-26. PubMed ID: 10521838
[TBL] [Abstract][Full Text] [Related]
23. Cytogenetic results from the U.S. Collaborative Study on CVS.
Ledbetter DH; Zachary JM; Simpson JL; Golbus MS; Pergament E; Jackson L; Mahoney MJ; Desnick RJ; Schulman J; Copeland KL
Prenat Diagn; 1992 May; 12(5):317-45. PubMed ID: 1523201
[TBL] [Abstract][Full Text] [Related]
24. Chromosomal microarray analysis on uncultured chorionic villus sampling can be complicated by confined placental mosaicism for aneuploidy and microdeletions.
Gu S; Jernegan M; Van den Veyver IB; Peacock S; Smith J; Breman A
Prenat Diagn; 2018 Oct; 38(11):858-865. PubMed ID: 30094853
[TBL] [Abstract][Full Text] [Related]
25. Whole-genome array CGH evaluation for replacing prenatal karyotyping in Hong Kong.
Kan AS; Lau ET; Tang WF; Chan SS; Ding SC; Chan KY; Lee CP; Hui PW; Chung BH; Leung KY; Ma T; Leung WC; Tang MH
PLoS One; 2014; 9(2):e87988. PubMed ID: 24505343
[TBL] [Abstract][Full Text] [Related]
26. First-trimester prenatal diagnosis performed on pregnant women with fetal ultrasound abnormalities: the reliability of interphase fluorescence in situ hybridization (FISH) on mesenchymal core for the main aneuploidies.
Toutain J; Epiney M; Begorre M; Dessuant H; Vandenbossche F; Horovitz J; Saura R
Eur J Obstet Gynecol Reprod Biol; 2010 Apr; 149(2):143-6. PubMed ID: 20045588
[TBL] [Abstract][Full Text] [Related]
27. Rapid diagnosis of pseudomosaicism in a case of Level II mosaicism for trisomy 5 in a single colony from an in situ culture of amniocytes and a review of mosaic trisomy 5 at amniocentesis.
Chen CP; Chang SJ; Chern SR; Wu PS; Chen YN; Chen SW; Yang CW; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2016 Aug; 55(4):602-3. PubMed ID: 27590391
[TBL] [Abstract][Full Text] [Related]
28. Dilemmas in Prenatal Chromosomal Diagnosis Revealed Through a Single Center's 30 Years' Experience and 90,000 Cases.
Konialis C; Pangalos C
Fetal Diagn Ther; 2015; 38(3):218-32. PubMed ID: 25659342
[TBL] [Abstract][Full Text] [Related]
29. Comparative genomic hybridization: a new approach to screening for intrauterine complete or mosaic aneuploidy.
Lestou VS; Desilets V; Lomax BL; Barrett IJ; Wilson RD; Langlois S; Kalousek DK
Am J Med Genet; 2000 Jun; 92(4):281-4. PubMed ID: 10842297
[TBL] [Abstract][Full Text] [Related]
30. [Rapid prenatal diagnosis of chromosome aneuploidies in 60 uncultured amniotic fluid samples by fluorescence in situ hybridization].
Wang H; Li H; Wang H; Wang H; Xia Y; Wen J; Long Z; Dai H; Liang D; Xia J; Wu L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):538-41. PubMed ID: 18841567
[TBL] [Abstract][Full Text] [Related]
31. aCGH on chorionic villi mirrors the complexity of fetoplacental mosaicism in prenatal diagnosis.
Filges I; Kang A; Klug V; Wenzel F; Heinimann K; Tercanli S; Miny P
Prenat Diagn; 2011 May; 31(5):473-8. PubMed ID: 21351283
[TBL] [Abstract][Full Text] [Related]
32. Clinical utility of array comparative genomic hybridization for detection of chromosomal abnormalities in pediatric acute lymphoblastic leukemia.
Rabin KR; Man TK; Yu A; Folsom MR; Zhao YJ; Rao PH; Plon SE; Naeem RC
Pediatr Blood Cancer; 2008 Aug; 51(2):171-7. PubMed ID: 18253961
[TBL] [Abstract][Full Text] [Related]
33. Role of FISH on uncultured amniocytes for the diagnosis of aneuploidies in the presence of fetal anomalies.
Locatelli A; Mariani S; Ciriello E; Dalprà L; Villa N; Sala E; Vergani P
Fetal Diagn Ther; 2005; 20(1):1-4. PubMed ID: 15608449
[TBL] [Abstract][Full Text] [Related]
34. [Application of multiplex ligation-dependent probe amplification for rapid detection of aneuploidies and structural chromosomal abnormalities in prenatal diagnosis].
Zhang J; Hu P; Luo C; Ji Q; Zhou J; Liu A; Ma D; Xu Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Feb; 31(1):11-5. PubMed ID: 24510553
[TBL] [Abstract][Full Text] [Related]
35. Prospective chromosome analysis of 3429 amniocentesis samples in China using copy number variation sequencing.
Wang J; Chen L; Zhou C; Wang L; Xie H; Xiao Y; Zhu H; Hu T; Zhang Z; Zhu Q; Liu Z; Liu S; Wang H; Xu M; Ren Z; Yu F; Cram DS; Liu H
Am J Obstet Gynecol; 2018 Sep; 219(3):287.e1-287.e18. PubMed ID: 29852155
[TBL] [Abstract][Full Text] [Related]
36. Interpreting mosaicism in chorionic villi: results of a monocentric series of 1001 mosaics in chorionic villi with follow-up amniocentesis.
Malvestiti F; Agrati C; Grimi B; Pompilii E; Izzi C; Martinoni L; Gaetani E; Liuti MR; Trotta A; Maggi F; Simoni G; Grati FR
Prenat Diagn; 2015 Nov; 35(11):1117-27. PubMed ID: 26213308
[TBL] [Abstract][Full Text] [Related]
37. Rapid prenatal diagnosis of chromosome aneuploidies by interphase fluorescence in situ hybridization: a one-year clinical experience with high-risk and urgent fetal and postnatal samples.
Bryndorf T; Lundsteen C; Lamb A; Christensen B; Philip J
Acta Obstet Gynecol Scand; 2000 Jan; 79(1):8-14. PubMed ID: 10646809
[TBL] [Abstract][Full Text] [Related]
38. Chorionic villus sampling (CVS) and fluorescence in situ hybridization (FISH) for a rapid first-trimester prenatal diagnosis.
Goumy C; Bonnet-Dupeyron MN; Cherasse Y; Laurichesse H; Jaffray JY; Lacroute G; Geneix A; Lemery D; Vago P
Prenat Diagn; 2004 Apr; 24(4):249-56. PubMed ID: 15065097
[TBL] [Abstract][Full Text] [Related]
39. Interphase fluorescence in situ hybridization characterization of mosaicism using uncultured amniocytes and cultured stimulated cord blood lymphocytes in prenatally detected Pallister-Killian syndrome.
Chen CP; Peng CR; Chern SR; Kuo YL; Wu PS; Town DD; Pan CW; Yang CW; Wang W
Taiwan J Obstet Gynecol; 2014 Dec; 53(4):566-71. PubMed ID: 25510702
[TBL] [Abstract][Full Text] [Related]
40. Inverted duplication, triplication and quintuplication through sequential breakage-fusion-bridge events induced by a terminal deletion at 5p in a case of spontaneous abortion.
Chai H; Grommisch B; DiAdamo A; Wen J; Hui P; Li P
Mol Genet Genomic Med; 2019 Oct; 7(10):e00965. PubMed ID: 31478360
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]