951 related articles for article (PubMed ID: 26833920)
21. Copy number variation sequencing-based prenatal diagnosis using cell-free fetal DNA in amniotic fluid.
Qi Q; Lu S; Zhou X; Yao F; Hao N; Yin G; Li W; Bai J; Li N; Cram DS
Prenat Diagn; 2016 Jun; 36(6):576-83. PubMed ID: 27084671
[TBL] [Abstract][Full Text] [Related]
22. Traditional karyotyping vs copy number variation sequencing for detection of chromosomal abnormalities associated with spontaneous miscarriage.
Liu S; Song L; Cram DS; Xiong L; Wang K; Wu R; Liu J; Deng K; Jia B; Zhong M; Yang F
Ultrasound Obstet Gynecol; 2015 Oct; 46(4):472-7. PubMed ID: 25767059
[TBL] [Abstract][Full Text] [Related]
23. Chromosomal abnormalities detected by karyotyping and microarray analysis in twins with structural anomalies.
Li L; He Z; Huang X; Lin S; Wu J; Huang L; Wan Y; Fang Q
Ultrasound Obstet Gynecol; 2020 Apr; 55(4):502-509. PubMed ID: 30977228
[TBL] [Abstract][Full Text] [Related]
24. Identification of Novel Congenital Heart Disease Candidate Genes Using Chromosome Microarray.
Shanshen E; Rosenberg J; Van Bergen AH
Pediatr Cardiol; 2018 Jan; 39(1):148-159. PubMed ID: 28993849
[TBL] [Abstract][Full Text] [Related]
25. Genetic anomalies in fetuses with tetralogy of Fallot by using high-definition chromosomal microarray analysis.
Peng R; Zheng J; Xie HN; He M; Lin MF
Cardiovasc Ultrasound; 2019 May; 17(1):8. PubMed ID: 31060568
[TBL] [Abstract][Full Text] [Related]
26. Application of next-generation sequencing for the diagnosis of fetuses with congenital heart defects.
Qiao F; Hu P; Xu Z
Curr Opin Obstet Gynecol; 2019 Apr; 31(2):132-138. PubMed ID: 30608255
[TBL] [Abstract][Full Text] [Related]
27. Diagnosis of fetal submicroscopic chromosomal abnormalities in failed array CGH samples: copy number by sequencing as an alternative to microarrays for invasive fetal testing.
Cohen K; Tzika A; Wood H; Berri S; Roberts P; Mason G; Sheridan E
Ultrasound Obstet Gynecol; 2015 Apr; 45(4):394-401. PubMed ID: 25510919
[TBL] [Abstract][Full Text] [Related]
28. Analysis of tissue from pregnancy loss and aborted fetus with ultrasound anomaly using subtelomeric MLPA and chromosomal array analysis.
Lou J; Sun M; Zhao Y; Fu Y; Yuan H; Dai Y; Liang F; He Y; Liu Y
J Matern Fetal Neonatal Med; 2022 Aug; 35(16):3064-3069. PubMed ID: 32811234
[TBL] [Abstract][Full Text] [Related]
29. Estimating the frequency of causal genetic variants in foetuses with congenital heart defects: a Chinese cohort study.
Lu F; Xue P; Zhang B; Wang J; Yu B; Liu J
Orphanet J Rare Dis; 2022 Jan; 17(1):2. PubMed ID: 34983622
[TBL] [Abstract][Full Text] [Related]
30. Clinical application of chromosomal microarray analysis in fetuses with increased nuchal translucency and normal karyotype.
Su L; Huang H; An G; Cai M; Wu X; Li Y; Xie X; Lin Y; Wang M; Xu L
Mol Genet Genomic Med; 2019 Aug; 7(8):e811. PubMed ID: 31209990
[TBL] [Abstract][Full Text] [Related]
31. Chromosome microarray testing for patients with congenital heart defects reveals novel disease causing loci and high diagnostic yield.
Geng J; Picker J; Zheng Z; Zhang X; Wang J; Hisama F; Brown DW; Mullen MP; Harris D; Stoler J; Seman A; Miller DT; Fu Q; Roberts AE; Shen Y
BMC Genomics; 2014 Dec; 15(1):1127. PubMed ID: 25516202
[TBL] [Abstract][Full Text] [Related]
32. Prenatal detection of chromosomal abnormalities and copy number variants in fetuses with congenital gastrointestinal obstruction.
Meng X; Jiang L
BMC Pregnancy Childbirth; 2022 Jan; 22(1):50. PubMed ID: 35045821
[TBL] [Abstract][Full Text] [Related]
33. Prenatal genetic diagnosis using microarray analysis in fetuses with congenital heart defects.
Schmid M; Stary S; Blaicher W; Gollinger M; Husslein P; Streubel B
Prenat Diagn; 2012 Apr; 32(4):376-82. PubMed ID: 22025351
[TBL] [Abstract][Full Text] [Related]
34. [Application of chromosome microarray analysis for fetuses with increased nuchal translucency and a normal karyotype].
Yang X; Fu F; Li R; Zhang Y; Wan J; Yang X; Han J; Pan M; Zhen L; Liao C
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Jun; 32(3):370-4. PubMed ID: 26037353
[TBL] [Abstract][Full Text] [Related]
35. Application of chromosomal microarray in fetuses with increased nuchal translucency.
Zhao XR; Gao L; Wu Y; Wang YL
J Matern Fetal Neonatal Med; 2020 May; 33(10):1749-1754. PubMed ID: 30688128
[No Abstract] [Full Text] [Related]
36. The Value of a Comprehensive Genomic Evaluation in Prenatal Diagnosis of Genetic Diseases: A Retrospective Study.
Fu F; Li R; Yu QX; Dang X; Yan SJ; Zhou H; Cheng K; Huang RB; Wang Y; Zhang YL; Jing XY; Zhang LN; Li DZ; Liao C
Genes (Basel); 2022 Dec; 13(12):. PubMed ID: 36553632
[TBL] [Abstract][Full Text] [Related]
37. Clinical aspects of prenatally detected congenital heart malformations and the yield of chromosomal microarray analysis.
Sukenik-Halevy R; Sukenik S; Koifman A; Alpert Y; Hershkovitz R; Levi A; Biron-Shental T
Prenat Diagn; 2016 Dec; 36(13):1185-1191. PubMed ID: 27794172
[TBL] [Abstract][Full Text] [Related]
38. Prenatal diagnosis of submicroscopic chromosomal aberrations in fetuses with congenital cystic adenomatoid malformation by chromosomal microarray analysis.
Deng Q; Huang L; Liu J; Fang F; Liu Z; Zhang Y; Li F; Liao C
J Matern Fetal Neonatal Med; 2021 Aug; 34(16):2623-2629. PubMed ID: 31581877
[TBL] [Abstract][Full Text] [Related]
39. Prenatal Diagnosis of BACs-on-Beads Assay in 3647 Cases of Amniotic Fluid Cells.
Li C; Chen B; Zheng J; Cheng L; Song T; Guo F; Xu H; Yan F; Xu Y; Li Y; Zhang J
Reprod Sci; 2019 Jul; 26(7):1005-1012. PubMed ID: 30326779
[TBL] [Abstract][Full Text] [Related]
40. Pathogenic recurrent copy number variants in 7,078 pregnancies via chromosomal microarray analysis.
Kang H; Chen Y; Wang L; Gao C; Li X; Hu Y
J Perinat Med; 2024 Feb; 52(2):171-180. PubMed ID: 38081620
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
