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.
150 related articles for article (PubMed ID: 38710614)
41. Microarray analysis in pregnancies with isolated echogenic bowel. Singer A; Maya I; Koifman A; Nasser Samra N; Baris HN; Falik-Zaccai T; Ben Shachar S; Sagi-Dain L Early Hum Dev; 2018 Apr; 119():25-28. PubMed ID: 29522884 [TBL] [Abstract][Full Text] [Related]
42. 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]
44. Performance of Chromosomal Microarray Analysis for Detection of Copy Number Variations in Fetal Echogenic Bowel. Fan X; Huang H; Lin X; Xue H; Cai M; Lin N; Xu L Risk Manag Healthc Policy; 2021; 14():1431-1438. PubMed ID: 33859509 [TBL] [Abstract][Full Text] [Related]
45. What have we learned from 691 prenatal chromosomal microarrays for ventricular septal defects? Maya I; Singer A; Yonath H; Reches A; Rienstein S; Zeligson S; Ben Shachar S; Sagi-Dain L Acta Obstet Gynecol Scand; 2020 Jun; 99(6):757-764. PubMed ID: 31424084 [TBL] [Abstract][Full Text] [Related]
46. Genetic diagnosis of common fetal renal abnormalities detected on prenatal ultrasound. Liu L; Li J; Li Y; Li H; Yang B; Fan H; Wang J; Gu Y; Yu H; Bai M; Yu T; Cui S; Cheng G; Ren C Prenat Diagn; 2022 Jun; 42(7):894-900. PubMed ID: 35478332 [TBL] [Abstract][Full Text] [Related]
47. Prenatal diagnosis for fetuses with isolated and non-isolated congenital heart defects using chromosomal microarray and exome sequencing. Xing Y; Zhang Y; Chen J; Wu F; Yuan M; Zou G; Yang Y; Zhou F; Zhou J; Sun L Prenat Diagn; 2022 Jun; 42(7):873-880. PubMed ID: 35584285 [TBL] [Abstract][Full Text] [Related]
48. Concordance of Chromosomal Microarray Analysis in Prenatal Diagnosis of Fetuses with Abnormal Ultrasonographic Soft Markers. Lu Y; Liu C; Ji Y J Coll Physicians Surg Pak; 2023 Mar; 33(3):270-274. PubMed ID: 36945155 [TBL] [Abstract][Full Text] [Related]
49. Prenatal diagnosis of chromosomal aberrations by chromosomal microarray analysis in fetuses with ultrasound anomalies in the urinary system. Hu T; Zhang Z; Wang J; Li Q; Zhu H; Lai Y; Wang H; Liu S Prenat Diagn; 2019 Nov; 39(12):1096-1106. PubMed ID: 31461547 [TBL] [Abstract][Full Text] [Related]
51. [Prenatal genetic diagnosis of the fetuses with isolated corpus callosum abnormality]. She Q; Zhen L; Fu F; Lei TY; Li LS; Li R; Wang D; Zhang YL; Jing XY; Yi CX; Zhong HZ; Tan WH; Li FG; Liao C Zhonghua Fu Chan Ke Za Zhi; 2022 Sep; 57(9):671-677. PubMed ID: 36177578 [No Abstract] [Full Text] [Related]
52. Chromosomal microarray should be performed for cases of fetal short long bones detected prenatally. Tzadikevitch Geffen K; Singer A; Maya I; Sagi-Dain L; Khayat M; Ben-Shachar S; Daum H; Michaelson-Cohen R; Feingold-Zadok M; Sukenik Halevy R Arch Gynecol Obstet; 2021 Jan; 303(1):85-92. PubMed ID: 32761367 [TBL] [Abstract][Full Text] [Related]
53. [Analysis of copy number variation by CMA in fetus with increased nuchal translucency]. Du L; Xie HN; Zheng J; He M Zhonghua Fu Chan Ke Za Zhi; 2018 Oct; 53(10):671-676. PubMed ID: 30369122 [No Abstract] [Full Text] [Related]
54. 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]
55. Is polyhydramnios in an ultrasonographically normal fetus an indication for genetic evaluation? Barnhard Y; Bar-Hava I; Divon MY Am J Obstet Gynecol; 1995 Nov; 173(5):1523-7. PubMed ID: 7503195 [TBL] [Abstract][Full Text] [Related]
56. Prenatal Diagnosis of Chromosomal Mosaicism in 18,369 Cases of Amniocentesis. Kang H; Wang L; Xie Y; Chen Y; Gao C; Li X; Hu Y; Liu Q Am J Perinatol; 2024 May; 41(S 01):e2058-e2068. PubMed ID: 37336233 [TBL] [Abstract][Full Text] [Related]
58. [Prenatal diagnosis and clinical outcomes of 297 fetuses with conotruncal defects]. Cao Q; Xu LL; Li R; Han J; Yi CX; Jing XY; Zhang LN; Li DZ; Pan M Zhonghua Fu Chan Ke Za Zhi; 2022 Jan; 57(1):25-31. PubMed ID: 35090242 [No Abstract] [Full Text] [Related]
59. [Application value of chromosome microarray analysis for prenatal diagnosis of fetus with ultrasonic abnormalities]. Mi X; Shen X; Zhang S Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Jan; 37(1):67-70. PubMed ID: 31922601 [TBL] [Abstract][Full Text] [Related]
60. Should Prenatal Chromosomal Microarray Analysis Be Offered for Pulmonary Atresia? A Single-Center Retrospective Study in China. Wang Y; Ma C; Fu F; Zhou H; Cheng K; Huang R; Li R; Li D; Liao C Genes (Basel); 2023 Mar; 14(3):. PubMed ID: 36980994 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]